28590218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55700654-C-T

28590337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55700766-G-A

28590337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55700766-G-T

28590409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55700830-A-G

28590450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55700871-T-C

28590586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701199-G-A

28590586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701199-G-T

http://identifiers.org/hco/15/GRCh38#28590666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55701368-C-A

28590713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701413-C-G

28590713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701413-C-T

http://identifiers.org/hco/15/GRCh38#28590742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55701440-C-A

28590820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701513-G-T

28590855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701549-T-C

28590989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701679-G-A

28590989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701679-G-C

28591196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701924-G-T

28591502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55701937-G-T

28591652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55702081-T-G

28591670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55702100-C-G

28591670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55702100-C-T

28592563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55702904-C-T

28592584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55702925-C-T

28592846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55703371-T-C

28592949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55703466-G-C

28592949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55703466-G-T

http://identifiers.org/hco/15/GRCh38#28593343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55704739-C-A

28593347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55704743-C-G

28593347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55704743-C-T

28593355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55704750-G-A

28593558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55704905-A-G

28593562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55704908-T-C

28593692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55705025-T-G

28593783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55705109-G-A

28593783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55705109-G-C

28593783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55705109-G-T

28594105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55705392-A-G

28600977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55710375-G-A

28601330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55711250-T-A

28601448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55711356-C-T

28612143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55717816-A-G

28613478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55718699-C-G

28617371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55720812-T-C

28617371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55720812-T-G

28617427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55720866-G-A

28617924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721391-A-G

28617971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721437-A-G

28618028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721519-G-T

28618088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55721612-T-G

28618534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55722051-C-T

28618619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 55722142-T-C

28628896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743332-G-A

28628897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743333-G-T

28629078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743837-A-G

28629132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743864-G-A

28629154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743886-G-T

28629194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743934-G-C

28629208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743955-C-G

28629213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743960-T-C

28629213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55743960-T-G

28629450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55744195-A-G

28629974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55745610-C-G

28630192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55745853-C-G

28630238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55745899-G-A

28630238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55745899-G-C

28630307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55745958-G-T

28630622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55746315-G-A

28630622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55746315-G-T

28630758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55746493-G-A

28630765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55746500-A-G

http://identifiers.org/hco/15/GRCh38#28632725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#55781005-A-C

28632886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781169-T-G

http://identifiers.org/hco/15/GRCh38#28632889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55781172-C-A

28632889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781172-C-T

28632993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781274-T-G

28633146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55781501-G-A

28633146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55781501-G-T

28633220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55781575-A-G

28633329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781765-G-T

http://identifiers.org/hco/15/GRCh38#28633373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55781846-C-A

28633373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781846-C-G

28633373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781846-C-T

28633404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781919-G-T

28633410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55781995-G-T

28633640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55782220-T-C

28633640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55782220-T-G

28635321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782489-C-T

28635328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782496-G-T

28635434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782597-C-G

28635436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782599-A-G

28635436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782599-A-T

28635457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782611-C-T

28635544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782696-A-G

28635616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782759-T-A

28635644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55782785-G-A

28635783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55783006-C-T

28635963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55783168-G-A

28636474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55784331-G-T

28636500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55784357-A-G

28636503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55784360-C-T

http://identifiers.org/hco/15/GRCh38#28636509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#55784366-C-A

28636804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784608-G-C

28636804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784608-G-T

28636818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784622-T-C

28636839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784647-A-G

28636890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784696-A-G

28636911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784717-T-G

28636926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784731-A-G

28636945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784749-T-C

28636951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784755-T-C

28636959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55784763-G-A

http://identifiers.org/hco/15/GRCh38#28637052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#55784856-C-A

28637115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55784919-G-C

28637118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55784922-C-G

28637118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55784922-C-T

28637128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55784932-G-T

http://identifiers.org/hco/15/GRCh38#28637359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55785163-C-A

28637359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55785163-C-G

28637359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55785163-C-T

28637422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55785221-G-A

28637659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55785458-A-G

28637904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55785623-G-A

28640245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786321-G-T

28640246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786322-T-C

28640377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55786453-A-G

28640403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786479-T-C

28640416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786492-A-G

28640416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786492-A-T

28640424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786499-T-A

28640424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786499-T-C

28640429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786504-A-G

http://identifiers.org/hco/15/GRCh38#28640482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55786553-C-A

28640544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786621-A-G

28640646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786727-T-C

28640829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55786877-A-G

http://identifiers.org/hco/15/GRCh38#28641083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787133-A-C

28641083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787133-A-G

28641324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787365-G-A

28641324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787365-G-T

28641326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787367-A-G

28641326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787367-A-T

http://identifiers.org/hco/15/GRCh38#28641356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787394-C-A

28641356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787394-C-T

28641394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787432-G-A

28641394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787432-G-T

http://identifiers.org/hco/15/GRCh38#28641405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787443-C-A

http://identifiers.org/hco/15/GRCh38#28641411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787449-C-A

28641415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787453-A-G

28641418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787456-T-A

28641418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787456-T-G

http://identifiers.org/hco/15/GRCh38#28641433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787471-A-C

28641433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787471-A-G

28641433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787471-A-T

28641436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787474-T-A

28641436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787474-T-C

28641478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787516-T-C

http://identifiers.org/hco/15/GRCh38#28641499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787537-C-A

28641499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55787537-C-T

28641592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787641-A-G

28641632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787710-T-C

28641638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787716-G-A

http://identifiers.org/hco/15/GRCh38#28641675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55787754-C-A

28641675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55787754-C-G

28642340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55788495-C-G

http://identifiers.org/hco/15/GRCh38#28642618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55788871-A-C

28642632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55788885-T-C

28642660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55788957-T-C

28642678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55788991-G-A

28642678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55788991-G-T

28642687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55789015-G-A

28642825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55789151-C-G

28642880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55789205-G-T

28642901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55789226-C-T

28643028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55789334-G-A

28643089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55789393-A-G

28644040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55790643-G-T

28648995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55795627-G-A

28649028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 55795660-A-G

28649120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55795738-A-G

28649137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55795754-T-G

28650725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55796503-T-A

28650731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55796509-G-A

http://identifiers.org/hco/15/GRCh38#28650732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55796510-C-A

28651528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55798510-C-G

28651705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55798715-G-A

28651882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55798843-G-A

28651973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55798887-A-G

28653023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801068-C-T

28653063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801122-G-A

28653147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801199-G-A

28653181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801231-G-A

28653181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801231-G-T

28653336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801402-G-A

28653367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801428-G-T

28653411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55801473-G-A

http://identifiers.org/hco/15/GRCh38#28653917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55801982-A-C

http://identifiers.org/hco/15/GRCh38#28654100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802042-C-A

28654117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802059-A-G

http://identifiers.org/hco/15/GRCh38#28654190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802105-A-C

28654227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802148-T-G

http://identifiers.org/hco/15/GRCh38#28654246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802164-C-A

http://identifiers.org/hco/15/GRCh38#28654252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802170-A-C

28654252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802170-A-G

28654256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802174-C-T

28654297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802214-A-G

28654297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802214-A-T

28654347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802264-T-C

28654347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802264-T-G

http://identifiers.org/hco/15/GRCh38#28654401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802318-C-A

28654401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802318-C-T

28654461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802378-G-A

28654486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802403-T-A

28654486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802403-T-C

28654488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802405-A-G

28654501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802416-T-A

28654501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802416-T-C

28654533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802447-G-A

28654533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802447-G-T

28654560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802466-G-A

28654560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802466-G-C

28654560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802466-G-T

28654863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802706-C-T

http://identifiers.org/hco/15/GRCh38#28655192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802725-A-C

http://identifiers.org/hco/15/GRCh38#28655210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55802743-C-A

28655210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802743-C-G

28655210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55802743-C-T

28655265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55802784-T-C

28655410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802929-G-A

28655410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55802929-G-T

28655423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802942-G-A

28655423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802942-G-C

28655423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802942-G-T

28655440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802965-C-T

28655450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802974-T-C

28655464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802989-G-A

28655464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55802989-G-T

28655559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55803078-A-G

http://identifiers.org/hco/15/GRCh38#28655601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55803120-C-A

http://identifiers.org/hco/15/GRCh38#28655652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55803171-C-A

28655652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55803171-C-T

28655954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55803683-G-A

28655954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55803683-G-T

28656043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55803771-T-C

28656057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55803779-A-T

http://identifiers.org/hco/15/GRCh38#28656967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55804530-C-A

28657015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804591-A-G

28657065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804650-A-G

28657122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804703-C-T

http://identifiers.org/hco/15/GRCh38#28657166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55804740-C-A

28657166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804740-C-T

28657314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55804890-A-G

28657314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55804890-A-T

http://identifiers.org/hco/15/GRCh38#28657328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55804904-C-A

28657328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804904-C-T

28657400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804964-G-A

28657400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55804964-G-T

28657436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805000-G-A

28657605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805145-C-T

28657631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805167-G-T

28657970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805443-T-C

28657978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805451-C-G

28658021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805488-C-T

28658072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805537-G-C

28658085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805555-A-G

28658135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805616-G-T

28658174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805693-G-C

28658258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805802-G-A

28658317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805877-G-A

28658393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55805933-G-A

28658457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806000-G-A

28658457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806000-G-T

28658579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806090-T-A

28658579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806090-T-G

28658619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55806131-G-A

28658619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55806131-G-T

28658711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55806223-A-G

28658735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55806247-A-G

28658738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55806250-T-C

28658746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55806258-A-G

28658746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55806258-A-T

http://identifiers.org/hco/15/GRCh38#28658762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55806274-C-A

28658783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806306-T-A

28658783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806306-T-C

28658791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806316-T-C

http://identifiers.org/hco/15/GRCh38#28658875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55806412-C-A

28658875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806412-C-G

28658930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806458-G-A

28658989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806503-C-T

28659007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806521-G-A

28663336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806568-G-A

28663357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806587-A-G

28663567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806796-G-T

28666969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806832-C-T

28667046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806893-G-C

28667046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806893-G-T

28667127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55806967-G-A

28667426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55807269-T-C

28667496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55807338-G-A

28667496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55807338-G-C

28667496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55807338-G-T

http://identifiers.org/hco/15/GRCh38#28667643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55807478-C-A

28667643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55807478-C-T

28667658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55807493-G-C

28667661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55807496-G-A

28667686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55807521-G-A

http://identifiers.org/hco/15/GRCh38#28668034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55808208-A-C

28668322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55809187-T-C

28668370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809233-T-A

28668370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809233-T-C

http://identifiers.org/hco/15/GRCh38#28668374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55809237-C-A

28668374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809237-C-G

28668374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809237-C-T

28668378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809241-A-G

http://identifiers.org/hco/15/GRCh38#28668380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55809243-C-A

28668380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809243-C-T

28668404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809265-A-G

28668449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809315-C-T

http://identifiers.org/hco/15/GRCh38#28668455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55809321-C-A

28668459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809325-A-G

28668459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55809325-A-T

28671437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55813467-C-G

28671437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55813467-C-T

28671672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55813692-A-G

http://identifiers.org/hco/15/GRCh38#28671798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55813824-C-A

28673099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814153-T-G

28673130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814184-T-C

28673502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814500-A-G

28673502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814500-A-T

28673534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814534-A-T

28673689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55814679-A-G

28673722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55814712-T-A

28673722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55814712-T-C

28673722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55814712-T-G

http://identifiers.org/hco/15/GRCh38#28673819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55814812-C-A

28673819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814812-C-T

28673834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55814827-T-G

http://identifiers.org/hco/15/GRCh38#28673968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55814966-C-A

28673968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: non coding transcript exon variant
orthologous variants: 55814966-C-T

http://identifiers.org/hco/15/GRCh38#28679312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55838616-C-A

28679312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838616-C-T

http://identifiers.org/hco/15/GRCh38#28679317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55838611-C-A

28679372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838560-T-C

28679372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838560-T-G

28679471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55838467-G-A

28679525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55838413-C-T

28679569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55838369-C-T

28679872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838090-C-T

28679885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838079-C-T

http://identifiers.org/hco/15/GRCh38#28679953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55838009-C-A

28680002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55837962-C-T

28680789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835756-G-A

28681113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835453-T-C

28681273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835293-A-G

28681884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834884-C-T

28681969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834796-A-G

28681976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834789-T-C

http://identifiers.org/hco/15/GRCh38#28682045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55834736-C-A

28682045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834736-C-T

http://identifiers.org/hco/15/GRCh38#28682142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55834647-C-A

28682142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834647-C-T

28682178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834611-G-A

28682178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834611-G-T

http://identifiers.org/hco/15/GRCh38#28682181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55834608-A-C

28682181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30495
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55834608-A-G