51539054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, undefined
orthologous variants: 106666050-T-C

51539588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron variant
orthologous variants: 106665545-G-A

51540395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron variant
orthologous variants: 106664741-T-C

51540463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron variant
orthologous variants: 106664707-T-C

51540646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron variant
orthologous variants: 106664528-C-T

51540707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron variant
orthologous variants: 106664463-A-T

51540710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron variant
orthologous variants: 106664460-A-G

51543268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106662326-C-G

51543298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106662294-G-A

51544339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106660847-A-G

51545114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106660254-C-G

51559363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106649684-T-G

51559423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106649630-G-A

51559747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106649364-T-A

51559862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106649258-T-C

51560013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106649120-C-G

http://identifiers.org/hco/3/GRCh38#51560198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106648945-A-C

51560198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648945-A-G

51560367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648854-T-A

51560367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648854-T-C

51560435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648804-C-T

51560518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648705-G-A

51560518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648705-G-T

51560720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106648423-C-T

51567921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106646295-G-A

http://identifiers.org/hco/3/GRCh38#51567939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106646277-C-A

51567939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106646277-C-T

51567944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106646272-A-G

51568014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106646184-C-T

51568239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106645949-A-G

51568439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106645772-T-G

51568476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106645736-G-A

51571904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106642240-A-G

51573074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106641945-T-A

51573166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106641856-G-T

51578321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106639195-G-A

51578378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106639138-T-G

51584239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106636413-T-C

51584243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106636409-C-T

51585180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106634469-T-C

51585180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106634469-T-G

51589753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106631640-G-T

51590797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106630760-C-G

51590974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106630628-G-T

51591106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106630519-C-T

51591484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106629571-G-A

51591484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106629571-G-C

http://identifiers.org/hco/3/GRCh38#51591570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106629486-C-A

51592125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106629077-C-T

51592183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106629030-C-T

51620593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106603006-A-G

51620593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106603006-A-T

51620774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106602782-G-A

51621788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106602165-G-A

51621798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106602154-A-G

http://identifiers.org/hco/3/GRCh38#51621802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106602150-A-C

51621980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106601442-G-A

51626966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106600619-C-T

51627409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106600235-T-C

51627467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106600201-T-C

51627467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106600201-T-G

51627507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106600161-T-C

51627541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106600124-T-C

51627830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106599857-A-G

51627905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106599783-G-A

http://identifiers.org/hco/3/GRCh38#51629281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106597712-C-A

51629281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106597712-C-G

51629281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106597712-C-T

http://identifiers.org/hco/3/GRCh38#51629288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106597705-C-A

51629579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106597407-C-G

51629579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106597407-C-T

http://identifiers.org/hco/3/GRCh38#51630304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106596889-C-A

51630373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106596820-A-G

51630410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106596735-C-T

51630489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106596507-A-T

http://identifiers.org/hco/3/GRCh38#51630501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106596495-C-A

http://identifiers.org/hco/3/GRCh38#51630955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106596087-C-A

51630990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106596058-G-A

51630990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106596058-G-T

http://identifiers.org/hco/3/GRCh38#51631172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106595896-A-C

http://identifiers.org/hco/3/GRCh38#51633428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106595274-A-C

51633428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106595274-A-G

51633453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106595249-T-C

51633523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106595185-C-T

51635292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106593780-T-A

51635493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106593587-A-G

51635648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106593399-C-T

http://identifiers.org/hco/3/GRCh38#51637241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106590703-A-C

51637581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106590381-G-A

51637581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106590381-G-T

51637590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106590373-G-A

51637590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106590373-G-T

51637651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106590322-A-G

51637824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106590004-T-C

51638350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106589504-A-G

51638350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106589504-A-T

51638381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106589473-G-C

http://identifiers.org/hco/3/GRCh38#51638449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106589407-C-A

51638449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106589407-C-T

http://identifiers.org/hco/3/GRCh38#51638564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106589301-C-A

51638568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106589297-A-G

51638840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588928-T-C

51638882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588581-T-C

51638882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588581-T-G

http://identifiers.org/hco/3/GRCh38#51638922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106588542-C-A

51638922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588542-C-T

http://identifiers.org/hco/3/GRCh38#51638939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106588524-C-A

http://identifiers.org/hco/3/GRCh38#51638994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106588479-C-A

http://identifiers.org/hco/3/GRCh38#51639055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106588418-A-C

51639064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588409-A-G

51639215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588274-A-G

http://identifiers.org/hco/3/GRCh38#51639247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106588242-C-A

51639401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106588129-C-T

51639804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106587724-G-A

51639838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106587691-T-C

http://identifiers.org/hco/3/GRCh38#51639859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106587670-C-A

51639859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106587670-C-T

51639965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106587565-A-G

51640065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106587480-G-A

51640065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106587480-G-T

51640666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106586185-A-G

http://identifiers.org/hco/3/GRCh38#51641811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106585468-C-A

51641811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106585468-C-T

51641964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106585316-G-A

51642149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106585191-G-T

51642216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106585124-T-C

51642430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106584935-G-C

http://identifiers.org/hco/3/GRCh38#51642477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106584882-A-C

http://identifiers.org/hco/3/GRCh38#51642614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#106584754-A-C

51642614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106584754-A-G

51642617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106584747-C-T

51642662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106584704-C-T

51643118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106584389-C-G

51643325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106584094-G-A

51643491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106583805-A-G

http://identifiers.org/hco/3/GRCh38#51643834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106583111-C-A

51643834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106583111-C-T

http://identifiers.org/hco/3/GRCh38#51643943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106582996-C-A

51643943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106582996-C-T

51643975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 106582964-G-A

http://identifiers.org/hco/3/GRCh38#51644041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106582930-C-A

51644995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581496-C-T

http://identifiers.org/hco/3/GRCh38#51645260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106581230-C-A

51645260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581230-C-T

51645281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581209-T-G

http://identifiers.org/hco/3/GRCh38#51645290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106581199-C-A

51645290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581199-C-G

51645343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581137-A-G

51645344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581136-G-A

51645344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581136-G-T

http://identifiers.org/hco/3/GRCh38#51645345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106581135-C-A

51645345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581135-C-T

51645460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581019-G-T

51645479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106581002-G-A

51645535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580928-A-G

51645535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580928-A-T

51645551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580908-A-G

51645578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580874-T-A

51645578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580874-T-G

51645867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580590-G-T

51645873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580584-T-C

51645873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580584-T-G

51646019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580402-G-T

51646238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580096-C-G

51646238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580096-C-T

51646240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580094-A-G

51646242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106580092-C-T

51646417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106579906-G-A

51646487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106579836-T-C

http://identifiers.org/hco/3/GRCh38#51646511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106579818-C-A

51646511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106579818-C-T

http://identifiers.org/hco/3/GRCh38#51646557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106579775-A-C

51646573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106579759-T-A

51655713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106578078-C-T

51655825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106578015-G-T

51655979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106577883-C-T

51656423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106576565-T-C

51656473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106576514-G-A

51656583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106576406-G-A

51656602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106576384-C-T

51657663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106575321-A-T

51657687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106575297-G-C

51657687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106575297-G-T

51657723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106575276-G-T

51657767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106575232-G-T

51658500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106574466-A-G

51658840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106574209-T-G

51659142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106573988-G-T

51659226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106573915-C-T

51659291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106573874-G-C

http://identifiers.org/hco/3/GRCh38#51659560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106573589-C-A

51659899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106573277-G-C

51659899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106573277-G-T

51660203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106572993-T-C

51661712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106572233-T-C

51662137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106571486-C-T

http://identifiers.org/hco/3/GRCh38#51662334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106570997-C-A

51662334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106570997-C-T

http://identifiers.org/hco/3/GRCh38#51662467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106570866-C-A

http://identifiers.org/hco/3/GRCh38#51662489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106570844-C-A

51662489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570844-C-G

51662489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570844-C-T

51662494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570839-G-A

51662566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570767-G-A

http://identifiers.org/hco/3/GRCh38#51662603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106570730-C-A

51662603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570730-C-G

51662606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570727-G-A

51662626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570707-G-A

51662816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570517-C-T

51663133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570200-C-G

51663223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570110-C-G

51663223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106570110-C-T

51663376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106569957-G-A

51663486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106569847-G-T

http://identifiers.org/hco/3/GRCh38#51663694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106569655-C-A

51663751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569602-A-G

51663764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569590-C-G

51663764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569590-C-T

51663765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569589-T-C

51663772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569582-A-G

51663772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569582-A-T

http://identifiers.org/hco/3/GRCh38#51663817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106569542-C-A

51663817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569542-C-G

51663817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569542-C-T

51664024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569322-G-A

51664024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569322-G-T

http://identifiers.org/hco/3/GRCh38#51664375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106569013-C-A

51664375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106569013-C-T

http://identifiers.org/hco/3/GRCh38#51664407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106568984-C-A

51664407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568984-C-T

51664705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568680-A-G

51664987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568383-C-T

http://identifiers.org/hco/3/GRCh38#51665060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106568302-A-C

51665060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568302-A-G

51665092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568265-T-C

51665161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568193-C-T

51665171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568183-G-C

51665171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106568183-G-T

51665662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567733-G-T

51665695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567700-G-T

51665697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567698-A-G

http://identifiers.org/hco/3/GRCh38#51666016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106567377-C-A

51666022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567371-A-G

http://identifiers.org/hco/3/GRCh38#51666137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106567260-A-C

51666137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567260-A-G

51666164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567232-A-G

51666164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567232-A-T

51666265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567171-G-A

51666282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567154-G-A

51666282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106567154-G-T

51666507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566955-G-C

http://identifiers.org/hco/3/GRCh38#51666540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106566925-C-A

51666540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566925-C-G

51666567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566898-T-C

51666570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566895-G-A

51667045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566547-G-C

51667066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566538-G-A

51667066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566538-G-C

51667066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566538-G-T

51667161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566452-C-T

http://identifiers.org/hco/3/GRCh38#51667573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106566345-C-A

http://identifiers.org/hco/3/GRCh38#51667602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106566325-C-A

51667739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566204-T-A

51667814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566130-G-T

51667825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106566119-G-A

http://identifiers.org/hco/3/GRCh38#51668233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#106565717-C-A

51668334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106565608-G-T

51668387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29123
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 106565555-G-T