104936497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811064-C-T

104936545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811112-T-C

104936545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811112-T-G

104936574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811141-T-C

104936594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811161-G-A

104936594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811161-G-T

104936639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42811206-G-A

104936766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 42811332-C-T

104937089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42811640-T-C

104937814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812537-C-T

104937844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812571-G-A

104937964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812728-T-C

104938105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812872-T-A

104938105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42812872-T-C

104938235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813022-A-G

104938292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813076-G-A

104938471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813255-G-A

104938503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813289-C-T

104938529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813326-T-A

104938858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813634-G-A

104938957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42813694-G-T

http://identifiers.org/hco/2/GRCh38#104939385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42814000-C-A

104939385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42814000-C-G

104939385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42814000-C-T

104940173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42814807-C-T

104940182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42814816-C-T

104940274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42815200-G-A

104941465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816837-C-T

104941542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816930-C-T

104941554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816942-T-C

104941558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816946-G-T

104941587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42816970-C-T

104941656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817037-A-G

104941673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817054-A-G

104941731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817099-G-T

104941744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817110-C-T

104941779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817142-C-T

104941791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817145-A-G

104941818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817165-T-C

104941818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817165-T-G

104942153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817496-G-A

104942190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817531-G-C

104942818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817807-T-C

104942921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42817911-A-T

104943139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818099-G-C

104943143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818103-A-G

104943973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818419-A-T

104944030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818474-C-T

http://identifiers.org/hco/2/GRCh38#104944085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42818519-C-A

104944248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818700-C-T

104944372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42818824-A-G

104944865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42819346-T-C

104944883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42819363-G-T

104944906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42819391-G-T

104944995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42819479-C-T

104945026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: non coding transcript exon variant
orthologous variants: 42819511-G-C

104945232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42819715-G-A

104945388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42819869-G-A

104945585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42820066-A-G

104945596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42820081-C-T

104945685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820166-G-A

104945701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820182-G-C

104945812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820282-A-G

104946244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820707-G-A

104946438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42820902-T-C

104946708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821175-G-A

104946730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821197-C-T

104946861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821290-C-T

104947019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821470-G-A

104947035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821486-G-A

104947035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42821486-G-C

104947702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822073-A-T

104947772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822147-G-A

104947806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822182-A-G

104947891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822261-G-A

104947937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822305-G-A

104948055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822416-G-A

104948396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822750-A-G

104948617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42822988-C-T

104949048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42825592-G-A

104949101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42825644-A-G

http://identifiers.org/hco/2/GRCh38#104949135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42825682-A-C

http://identifiers.org/hco/2/GRCh38#104950832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42829944-C-A

104951001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830440-G-A

104951057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830484-G-C

104951069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830496-A-T

104951100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830525-A-T

104951231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830629-A-T

104951462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830791-T-G

104951537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830860-C-T

http://identifiers.org/hco/2/GRCh38#104951653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42830970-C-A

104951653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830970-C-T

104951676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42830995-A-G

104966145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42835377-T-C

104967757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42840243-T-C

104967975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42840461-C-G

104968104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42840727-T-C

104968453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42841110-T-G

104968469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42841126-A-G

104968495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42841152-C-T

104968504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42841161-G-A

104968504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42841161-G-C

104968577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42841910-G-A

104968756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842095-G-A

104968884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842207-C-T

104968943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842238-C-G

104969023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842315-G-A

104969105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842397-G-A

104969135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842429-T-C

104969141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42842435-C-T

104969437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42843216-C-G

104969437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42843216-C-T

104969517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42843291-G-C

http://identifiers.org/hco/2/GRCh38#104969851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#42843695-C-A

104969851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42843695-C-G

104969950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42843778-C-T

104969990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42843813-C-T

104970049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42843868-A-G

104970707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844220-G-A

104970707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844220-G-T

104970763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844233-G-A

104970845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844265-A-G

104970948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844359-C-T

104970984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844395-G-A

104971001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42844412-T-G

104975597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42848621-G-A

http://identifiers.org/hco/2/GRCh38#104975603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42848629-A-C

104975603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42848629-A-G

104975691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42848701-T-C

104975691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42848701-T-G

104976701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42850447-C-T

104976738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42850490-G-A

104977143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42850832-G-A

http://identifiers.org/hco/2/GRCh38#104977302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42850999-A-C

104977827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42851661-G-T

http://identifiers.org/hco/2/GRCh38#104977913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42851758-C-A

http://identifiers.org/hco/2/GRCh38#104978024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42851858-C-A

104978324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852133-A-G

104978339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852148-T-A

104978415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852192-T-A

104978427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852204-T-G

104978430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852207-A-G

http://identifiers.org/hco/2/GRCh38#104978547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42852277-C-A

104978547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852277-C-T

104978634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852334-G-A

104978634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852334-G-T

104978652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852352-A-G

104978661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852361-T-G

104978663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852363-T-A

104978663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852363-T-G

104978721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852401-A-T

104978887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852563-T-C

104979143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42852818-A-G

104979399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42853060-C-T

104980469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42853169-A-G

104980667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42853358-G-C

104980977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42853770-C-T

104981209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854026-G-A

104981229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854046-G-A

104981238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854055-T-C

104981334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854161-C-G

104981334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854161-C-T

104981375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854201-C-G

104981587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854413-C-T

104981788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854617-G-A

104981837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42854675-C-T

http://identifiers.org/hco/2/GRCh38#104982256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42855004-C-A

104982394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42855104-T-C

104982716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42855351-G-A

104983543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42856196-A-G

104984012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42856353-G-A

104989177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42857355-G-T

104989568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42857763-C-T

104989704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42857899-G-C

104996562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42860804-G-A

104996616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42861326-G-A

104996849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42861565-A-G

104996884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42861599-A-G

104996990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42861706-A-G

104997054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42861770-G-A

104997127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42861843-A-T

104997454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42862135-G-A

http://identifiers.org/hco/2/GRCh38#104997481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42862147-C-A

104997481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42862147-C-T

http://identifiers.org/hco/2/GRCh38#104997745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42862396-A-C

104997774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42862413-A-G

104997927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42862552-T-C

105002826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42865436-C-T

105002898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42865518-A-G

105002938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42865559-T-C

105003460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42866103-T-C

105003463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42866106-T-G

105003528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42866162-T-C

105005845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42867758-G-T

105005885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42867799-A-G

105005919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42867834-G-A

105006075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42867969-C-T

105006076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42867970-C-T

http://identifiers.org/hco/2/GRCh38#105006093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42867992-A-C

105006239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868120-C-T

105006276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868154-A-G

105006352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868226-G-A

http://identifiers.org/hco/2/GRCh38#105006356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42868230-A-C

105006356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868230-A-G

105006356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868230-A-T

105006469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868730-G-A

105006549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868797-A-T

105006597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42868843-T-A

105006945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42870544-T-C

105006945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42870544-T-G

105007123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42870709-G-C

105007160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42870727-T-A

105007240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42870790-C-T

105010871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42872134-T-C

105011045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42872308-C-T

http://identifiers.org/hco/2/GRCh38#105011304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42872474-A-C

105015934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42873264-G-A

105015941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42873271-T-A

105016351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42873622-T-C

105016393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42873664-C-T

105016706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42873981-G-A

105016911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42874179-C-T

105016954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42874222-T-C

105022681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42877220-G-T

105022735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42877262-G-T

105022919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42877443-C-T

105022937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42877461-T-A

105023040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42877742-A-G

105023319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42878008-T-A

105023831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42878509-G-C

105023871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42878553-C-G

105024262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42878933-C-T

105024495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42879177-A-G

105024604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42879315-A-G

105024714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42879425-T-C

105025336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42880086-T-G

105025344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42880108-C-T

105026856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42881323-A-T

105027127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42881603-T-C

105027733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42881862-T-G

105027741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42881869-T-C

105027862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42881998-A-G

105027921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42882054-A-G

105027948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42882077-A-G

105027948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42882077-A-T

105037313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42889876-T-C

105037552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42890074-G-A

http://identifiers.org/hco/2/GRCh38#105037570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42890088-C-A

105037586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42890107-T-C

105037695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890190-G-C

105037728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42890204-G-A

105037728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42890204-G-C

105037941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890319-G-A

105037941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890319-G-T

http://identifiers.org/hco/2/GRCh38#105038044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#42890403-C-A

105038044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42890403-C-G

105038138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890497-C-T

105038190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890549-C-T

105038198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890557-C-T

http://identifiers.org/hco/2/GRCh38#105038303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#42890653-A-C

105038303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890653-A-G

105038303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890653-A-T

105038371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890694-G-A

105038371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890694-G-C

105038371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890694-G-T

105038382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890705-G-A

105038382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42890705-G-T

105038385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42890708-A-G

105038385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42890708-A-T

105038391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42890714-G-A

105038391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42890714-G-C

105038391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40687
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42890714-G-T