http://identifiers.org/hco/3/GRCh38#194005606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29767065-C-A

194005646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29767105-G-A

194005646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29767105-G-T

194005654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29767113-A-G

194005988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29768864-T-C

http://identifiers.org/hco/3/GRCh38#194005990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29768866-C-A

194006032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29768905-T-C

194006104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29768993-G-A

194006183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769069-A-T

194006757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769443-A-G

194006848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769541-C-T

194006859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769552-G-C

http://identifiers.org/hco/3/GRCh38#194006901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29769573-A-C

194007016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769708-A-G

194007069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769735-G-A

194007079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769745-C-T

194007223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769847-G-A

194007297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769931-A-G

194009362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771324-T-C

194009362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771324-T-G

194009374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771336-G-T

194009422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771390-T-A

194009422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29771390-T-C

http://identifiers.org/hco/3/GRCh38#194009552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29771498-C-A

194009604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29771554-G-A

194009616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29771567-A-G

194009632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29771589-T-A

194009905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29772846-A-G

http://identifiers.org/hco/3/GRCh38#194009978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29772909-C-A

194009978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29772909-C-T

194010120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773046-T-C

194010151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773074-G-A

194010337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773250-A-G

http://identifiers.org/hco/3/GRCh38#194010404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29773312-C-A

194010404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773312-C-G

194010474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773383-G-T

http://identifiers.org/hco/3/GRCh38#194010486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29773397-C-A

194010486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773397-C-T

http://identifiers.org/hco/3/GRCh38#194010487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29773398-C-A

194010487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29773398-C-T

194010576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29773484-A-G

194010668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773567-G-T

194010798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773694-G-A

194011017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773897-A-G

194011090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29774015-T-A

194012041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29774872-G-C

194012144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29774974-T-A

194012659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775533-C-T

194013060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775921-C-T

194013190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29776055-G-A

194013198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29776063-G-A

194014101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29777921-C-T

194014188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29777965-G-A

194014188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29777965-G-C

194014188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29777965-G-T

194014771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29778769-A-G

194015149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29779147-G-T

194015337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29779335-A-T

194015346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29779344-A-T

194015454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29779438-G-A

194015454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29779438-G-C

194015610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29779538-G-A

194015681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29779606-G-T

194015706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29779632-A-G

http://identifiers.org/hco/3/GRCh38#194015974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29779875-C-A

194015996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29779897-G-A

194016007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29779909-T-G

194016011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29779911-G-A

194016011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29779911-G-C

http://identifiers.org/hco/3/GRCh38#194016432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29780184-C-A

194016626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780342-T-C

194016924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780735-T-C

194017150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780905-G-A

194017221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780966-G-A

194017292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781025-A-T

194017398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781128-C-T

194017506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781239-A-G

194017628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781338-A-G

194017682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781390-G-A

194017730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29781437-A-G

http://identifiers.org/hco/3/GRCh38#194018272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29782253-C-A

194018272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782253-C-T

194018298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782267-C-T

194018347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782317-G-C

194018436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782393-A-G

http://identifiers.org/hco/3/GRCh38#194018497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29782430-A-C

194018627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782544-C-T

194018803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782691-C-T

194018804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782692-G-A

194018949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29782785-A-G

http://identifiers.org/hco/3/GRCh38#194019745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29784239-C-A

194019745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784239-C-G

194019776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784269-C-T

194019976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784474-G-A

194019976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784474-G-C

http://identifiers.org/hco/3/GRCh38#194020005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29784503-A-C

194020087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29784565-G-T

194020285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784771-G-A

194021616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785493-G-A

194021616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785493-G-C

194021616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785493-G-T

194021743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785594-A-G

194021861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29785712-C-T

194022112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29786181-G-T

http://identifiers.org/hco/3/GRCh38#194022265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29786435-A-C

194023072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787260-G-T

194023653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787837-T-C

194023719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29787886-T-C

194024047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788148-C-G

194024074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29788182-G-C

http://identifiers.org/hco/3/GRCh38#194026542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29789421-A-C

194026639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789506-T-C

194026740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789603-G-T

194026818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789657-C-T

http://identifiers.org/hco/3/GRCh38#194026995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29789806-C-A

194028677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790445-G-C

194028957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790694-A-G

194028965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790702-C-T

194029251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29790960-A-G

http://identifiers.org/hco/3/GRCh38#194029407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29791157-C-A

194029487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791221-T-C

194029508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791242-G-T

194029530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791266-T-C

194029632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791359-A-G

194029676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791394-T-C

http://identifiers.org/hco/3/GRCh38#194029693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29791411-C-A

194029693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791411-C-T

194029722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791460-G-T

http://identifiers.org/hco/3/GRCh38#194029723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29791461-C-A

194029723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29791461-C-G

http://identifiers.org/hco/3/GRCh38#194029724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29791462-C-A

http://identifiers.org/hco/3/GRCh38#194029845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29791610-C-A

http://identifiers.org/hco/3/GRCh38#194029870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29791634-A-C

194029882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29791646-G-T

194030122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29791879-A-T

http://identifiers.org/hco/3/GRCh38#194030428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29792169-C-A

194030475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792204-C-T

194031096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792515-A-G

194031396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792798-G-A

194031535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792921-T-A

194031535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792921-T-C

194031700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29793074-T-A

194031795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29793163-G-A

194031795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29793163-G-C

194032179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29793564-T-C

194032264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29793651-C-T

194032737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794282-G-A

194032737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794282-G-T

http://identifiers.org/hco/3/GRCh38#194032958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29794474-A-C

194032958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794474-A-T

194033009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794521-G-T

194033408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29794970-G-A

194033687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795128-G-T

194033750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795190-A-T

194034833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795900-G-A

http://identifiers.org/hco/3/GRCh38#194034837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29795904-A-C

194034901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795965-G-T

194035057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796117-C-T

194035256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796273-G-A

http://identifiers.org/hco/3/GRCh38#194035304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29796318-C-A

194035304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796318-C-T

194035581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796578-G-T

194035981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29796964-G-A

http://identifiers.org/hco/3/GRCh38#194036125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29797060-A-C

194036425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29797385-T-C

194036497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29797457-G-A

194036513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29797473-G-A

194036513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29797473-G-T

194036656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29797636-A-G

194036759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797701-G-T

194039034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29797850-C-T

194039132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29797949-C-T

194039241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798043-T-C

194039336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798125-G-A

194040586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798197-C-T

http://identifiers.org/hco/3/GRCh38#194040612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29798223-C-A

194040612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798223-C-T

194040738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798339-C-T

194040910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798518-T-G

194041037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798655-T-A

194041037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29798655-T-C

194041747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29799087-C-T

http://identifiers.org/hco/3/GRCh38#194042691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29799597-A-C

http://identifiers.org/hco/3/GRCh38#194042875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29799771-C-A

194042875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29799771-C-T

194042958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799855-G-T

194043072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799934-G-A

194043116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29799961-A-G

194043201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29800050-T-A

http://identifiers.org/hco/3/GRCh38#194043378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29800218-C-A

http://identifiers.org/hco/3/GRCh38#194043561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29800408-C-A

194043641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29800479-T-A

194043641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29800479-T-C

194043962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29802998-G-T

194044085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803129-A-G

194045240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803294-C-T

194045289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803348-C-T

194045429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803460-T-C

http://identifiers.org/hco/3/GRCh38#194045867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29803873-C-A

http://identifiers.org/hco/3/GRCh38#194046099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29804100-C-A

http://identifiers.org/hco/3/GRCh38#194046413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29804427-C-A

194046419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29804432-G-T

194046422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29804435-C-G

http://identifiers.org/hco/3/GRCh38#194046616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29804568-C-A

http://identifiers.org/hco/3/GRCh38#194046658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29804597-C-A

194046680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29804618-C-T

194046783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29804700-C-T

194046792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29804709-G-T

194046848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29804764-T-C

194046849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29804765-G-T

194047747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29805151-T-C

194047760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29805164-G-A

194048204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29806207-C-G

194048204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29806207-C-T

194048732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29806637-C-T

194049145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807038-A-G

194049145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807038-A-T

194049238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807131-G-A

194049239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807132-C-G

194049263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807156-A-G

194049263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807156-A-T

194049274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29807166-G-A

http://identifiers.org/hco/3/GRCh38#194049288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29807180-A-C

194049412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807230-C-T

http://identifiers.org/hco/3/GRCh38#194049413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29807231-C-A

194049413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807231-C-T

http://identifiers.org/hco/3/GRCh38#194049455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29807236-C-A

194049538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807319-T-C

194049593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807374-C-T

194049616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807397-A-G

194049676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807427-A-G

194049698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807449-T-C

194049955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29807702-G-T

194050394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29808308-G-A

http://identifiers.org/hco/3/GRCh38#194050500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29808420-C-A

194050547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29808467-T-C

194051732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29809614-C-T

194052017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29809910-C-T

http://identifiers.org/hco/3/GRCh38#194052174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29810063-C-A

194052217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810106-G-C

194052217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810106-G-T

194052229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810118-G-T

194052230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810119-T-C

http://identifiers.org/hco/3/GRCh38#194052233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29810122-C-A

194052233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810122-C-T

194052255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810148-G-T

194052374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29810255-G-C

194052374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29810255-G-T

194052603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810454-A-T

194052675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29810532-G-A

194053306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811139-T-A

194053374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811203-G-C

194053423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811239-T-C

194054495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29811963-G-A

194054495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29811963-G-C

194054495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29811963-G-T

194054533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29811996-C-T

194054616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812077-A-G

194054617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812078-G-T

194054629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812090-G-C

194054629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812090-G-T

194054816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812239-G-T

194054817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812240-G-T

194054827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812249-A-G

194054982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812349-G-A

194055071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812432-G-A

194055146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812542-G-A

194055147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812543-A-G

194055147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29812543-A-T

http://identifiers.org/hco/3/GRCh38#194055172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29812567-C-A

194055644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813003-T-C

194055883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813163-G-A

194056634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813703-T-C

194056666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813739-G-C

194056672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29813745-T-C

194056719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29813813-G-A

194056793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813925-C-G

http://identifiers.org/hco/3/GRCh38#194056837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29813968-C-A

194056842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29813973-T-A

194057075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29814194-C-T

194057799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29814597-T-C

194057910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29814672-G-A

194057943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29814703-A-G

194058009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29814756-C-G

194058047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29814785-T-A

http://identifiers.org/hco/3/GRCh38#194058209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29814949-C-A

194058209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29814949-C-T

194058222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29814959-A-G

194058244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29814981-T-C

194058267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29815004-C-T

194058349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29815035-G-C

194058394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29815077-G-A

194058858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815538-G-A

194058875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815553-T-G

194059039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29815719-G-C

194060311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818634-G-A

http://identifiers.org/hco/3/GRCh38#194061528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29820983-C-A

194061529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29820984-A-G

194061650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29821100-T-G

194061747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29821182-G-A

194061937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821336-T-C

194062066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821454-G-C

194062088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821476-C-T

194062097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821485-A-G

194062272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821594-C-T

194062279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821601-A-G

194062784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29821833-T-C

194062952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822058-T-C

194062952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822058-T-G

194063104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822179-T-G

194063197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822272-A-T

194063313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822393-T-A

194063313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822393-T-C

194063513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822554-C-T

194063515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29822556-T-C

194063906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823027-C-T

194063992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823142-A-T

194064027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823173-T-A

194064217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823418-A-G

http://identifiers.org/hco/3/GRCh38#194064671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29823886-A-C

194064671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823886-A-G

194064749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29823979-C-T

194064877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29824085-A-G

194065224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29824425-G-A

194065229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29824430-A-G

194065416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29824592-T-C

http://identifiers.org/hco/3/GRCh38#194065456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29824642-A-C

194065511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29824695-A-G

194065608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29824781-C-T

194065637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29824804-G-A

194065782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29824953-C-T

194065825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29824993-C-T

194065841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29825009-C-G

194066013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29825178-A-G

194066013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29825178-A-T

194070006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29826723-A-G

194070024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29826741-G-A

http://identifiers.org/hco/3/GRCh38#194070053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29826770-A-C

194070064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29826781-G-T

194070101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29826816-A-G

http://identifiers.org/hco/3/GRCh38#194070311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#29827050-C-A

194070311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29827050-C-T

http://identifiers.org/hco/3/GRCh38#194070333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29827076-C-A

194070333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29827076-C-T

194070341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827084-G-C

194070349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827092-G-A

194070349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827092-G-T

194070406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827146-T-C

194070409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827149-G-A

194070412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827152-T-C

http://identifiers.org/hco/3/GRCh38#194070437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29827177-C-A

194070437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827177-C-T

http://identifiers.org/hco/3/GRCh38#194070450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29827190-C-A

194070450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827190-C-T

http://identifiers.org/hco/3/GRCh38#194070554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#29827291-C-A

194070554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29827291-C-T

194070872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29827545-G-A

194070872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29827545-G-T

194070877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29827550-G-A

194070973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29827618-G-A

194070994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27718
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29827642-G-T