61680504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, undefined
orthologous variants: 10282183-G-T

61680607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10282090-C-T

61680697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281999-A-T

61680911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281792-G-A

61681038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281661-A-G

61681085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281614-C-T

61681185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281519-G-C

61681573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281198-G-A

61681718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10281099-C-G

61683735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10279338-A-G

61683846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10279232-G-T

61683881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10279199-G-T

61684011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10279066-A-G

61684048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10279029-C-G

61684343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10278732-T-C

61684581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10278536-T-A

61684581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10278536-T-C

61685290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10277864-C-T

61685293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10277861-G-A

61685455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10277730-C-G

61685794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10277477-A-G

61685927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10277365-A-G

61686314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10276988-C-T

61686598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10276666-G-A

61686740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10276526-C-T

61688668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10275053-G-A

61688668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10275053-G-T

61688816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10274905-G-A

61688876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10274851-G-A

61689234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10274457-C-T

http://identifiers.org/hco/11/GRCh38#61689323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10274349-C-A

61689323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10274349-C-T

61689503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10274178-C-T

http://identifiers.org/hco/11/GRCh38#61689547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10274143-C-A

61689547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10274143-C-T

61689834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10273718-T-C

61689860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10273678-G-A

61689962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10273571-C-T

61690363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10273245-G-C

61690839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10272847-G-A

61690839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10272847-G-T

61690937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10272750-G-A

61691561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10272113-G-A

61691602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10272079-G-C

61691680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271962-C-T

61691933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271773-C-T

61692190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271526-G-A

61692277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271447-G-A

61692277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271447-G-C

61692277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271447-G-T

61692360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271352-C-T

61692524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271244-C-T

61692748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10271116-A-G

61693680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10270449-G-A

61693790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10270322-C-T

61693835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10270271-G-A

61693842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10270264-C-T

61694084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10270038-C-G

61694434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10269734-G-A

61694550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10269638-C-T

61694755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10269499-A-G

61694783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10269471-G-A

61694808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10269446-A-G

61695036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10269211-C-G

61695036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10269211-C-T

61695044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10269206-G-C

61695360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10268921-G-A

61695398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10268894-A-G

61695505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10268843-T-G

61696033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10268309-G-A

http://identifiers.org/hco/11/GRCh38#61696053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10268291-C-A

61696160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10268183-C-T

61696251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10268090-T-C

61696341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10268005-G-C

61696418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10267968-C-G

http://identifiers.org/hco/11/GRCh38#61696943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10267449-C-A

61696943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10267449-C-T

61696973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10267418-T-C

61697429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10266920-C-T

http://identifiers.org/hco/11/GRCh38#61697897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10266442-A-C

61697969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10266368-G-A

61698843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10265565-T-G

61699024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10265429-C-T

61699159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10265330-G-A

61700590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10263446-A-T

61700804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262828-G-A

61701033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262596-T-A

61701033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262596-T-C

61701106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262528-A-T

61701119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262516-A-G

http://identifiers.org/hco/11/GRCh38#61701135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10262500-C-A

61701358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262267-A-G

61701387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10262241-C-T

61701537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10262084-G-A

61701539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10262082-G-A

61701539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10262082-G-C

61702625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10261615-G-A

61702756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10261494-G-A

61703039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10261263-G-A

61703482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10260888-T-G

61703678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10260731-A-G

61704981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10260258-T-C

61705148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10260146-C-T

61705525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259871-C-G

61705525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259871-C-T

61705587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259809-G-A

61705630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259757-T-C

61705847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259546-C-G

http://identifiers.org/hco/11/GRCh38#61706035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10259388-C-A

61706035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259388-C-T

61706145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259288-T-G

61706151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10259282-C-G

61706500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258960-C-T

61706518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258932-C-G

61706594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258847-C-G

61707209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258309-A-G

61707214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258304-A-G

61707256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258273-G-A

61707449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10258088-C-T

61707649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10257904-G-C

61707649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10257904-G-T

61707860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10257725-T-G

61707867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10257718-G-A

61709974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10256361-A-G

61710030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10256307-G-A

61710149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10256188-C-T

61710308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10256030-G-A

61710478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10255874-G-A

61710478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10255874-G-T

61710485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10255867-C-G

61710547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10255800-C-T

61710774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10255605-G-A

61711016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10255426-A-G

61711806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10254779-C-G

61711806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10254779-C-T

61711919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10254685-G-T

61712167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10254429-A-G

61712730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10253972-C-T

61714199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10253732-G-A

61715881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10253556-T-A

61716280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10253245-G-A

61716530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10253039-G-T

61716551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10253016-G-A

61716850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10252654-G-C

61717376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10251550-C-T

61717424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10251503-G-A

61717424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10251503-G-T

61717812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10251087-G-C

http://identifiers.org/hco/11/GRCh38#61718568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10250472-C-A

http://identifiers.org/hco/11/GRCh38#61718638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10250409-C-A

61718983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10250052-G-A

61718992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 10250042-G-A

61719239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249804-A-G

61719381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249699-A-G

61719992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249110-G-T

http://identifiers.org/hco/11/GRCh38#61720023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10249075-C-A

61720023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249075-C-T

61720038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249060-T-A

61720038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249060-T-C

61720038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10249060-T-G

61720128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10248977-C-T

61720269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248844-G-A

61720274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248839-C-T

61720554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248649-T-A

61720554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248649-T-C

61720554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248649-T-G

http://identifiers.org/hco/11/GRCh38#61720587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10248624-C-A

61720587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248624-C-T

61720639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248598-G-A

61720664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248573-G-A

61720908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248335-T-G

http://identifiers.org/hco/11/GRCh38#61720937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10248303-C-A

61720937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248303-C-T

61720938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10248302-T-C

http://identifiers.org/hco/11/GRCh38#61720944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10248289-C-A

61721718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10247888-T-C

61721767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10247854-G-A

http://identifiers.org/hco/11/GRCh38#61722789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10247258-C-A

http://identifiers.org/hco/11/GRCh38#61722790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10247257-C-A

61722790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10247257-C-T

http://identifiers.org/hco/11/GRCh38#61722828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10247222-C-A

http://identifiers.org/hco/11/GRCh38#61722849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10247190-C-A

61722849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10247190-C-G

61722964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10247075-C-T

http://identifiers.org/hco/11/GRCh38#61723067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10246988-C-A

61723084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246973-G-T

61723093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246971-G-A

61723093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246971-G-T

61723356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246763-T-C

http://identifiers.org/hco/11/GRCh38#61723408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10246715-C-A

61723416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246707-T-C

61723463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 10246658-C-T

61723596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246495-A-G

61723597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246494-G-T

61723631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10246460-G-T

61723895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10245573-A-G

61723900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10245568-A-G

61723973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10245508-T-G

61724370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10245010-T-G

61724464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10244945-C-T

61724682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10244766-C-T

61725864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10242576-C-G

61725864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10242576-C-T

61725938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10242513-C-T

61726172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10242290-G-A

61726172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10242290-G-T

http://identifiers.org/hco/11/GRCh38#61726406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10242112-C-A

61726408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10242110-C-G

61726540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10241992-C-T

61727320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10241320-C-T

61727358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10241283-G-C

http://identifiers.org/hco/11/GRCh38#61727652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10241026-C-A

61727856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240863-G-A

61727901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240834-C-T

61728003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240729-G-A

61728018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240714-T-C

61728029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240703-T-A

http://identifiers.org/hco/11/GRCh38#61728067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10240677-C-A

61728139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240609-C-T

61728246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10240497-C-T

61728341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240408-A-G

61728414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240349-T-C

61728514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10240317-C-T

61728515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10240316-G-A

61728607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240221-C-G

61728607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240221-C-T

61728687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240147-C-T

61728735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240099-G-A

61728770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240066-T-G

61728807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240030-G-A

61728807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240030-G-T

http://identifiers.org/hco/11/GRCh38#61728814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10240022-C-A

61728814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10240022-C-T

http://identifiers.org/hco/11/GRCh38#61728877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10239977-C-A

http://identifiers.org/hco/11/GRCh38#61728914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10239950-A-C

61729041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10239835-T-C

61729041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10239835-T-G

61729052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10239827-C-T

http://identifiers.org/hco/11/GRCh38#61729140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10239766-C-A

61729202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10239716-C-T

61729339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10239575-C-T

61729491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10239447-G-C

61730630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238737-C-T

61730674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238704-G-A

61730829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238576-G-C

61730861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10238543-C-T

61730970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238451-G-A

61730970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238451-G-C

61730970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238451-G-T

61731031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10238394-G-A

http://identifiers.org/hco/11/GRCh38#61731228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10238224-C-A

61731228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10238224-C-T

61731368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10238086-G-T

61731383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10238071-C-G

61731383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10238071-C-T

61731522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237912-T-C

61731552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237883-A-G

61731552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237883-A-T

http://identifiers.org/hco/11/GRCh38#61731583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10237855-C-A

61731583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237855-C-G

61731583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237855-C-T

61731865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237646-G-A

61731934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237577-G-A

61731980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237385-T-G

61731986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237379-A-G

61732028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237334-C-T

61732179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237189-T-G

http://identifiers.org/hco/11/GRCh38#61732315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10237082-C-A

61732380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10237024-A-G

61733498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10236028-A-G

61733683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10235842-T-A

61733710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10235816-C-G

61734025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10235443-G-A

61734233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10235048-G-A

61734528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10234647-G-A

61734734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10234448-G-T

61735038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10234147-G-A

61735038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10234147-G-C

61735045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10234140-G-A

61735145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10234076-A-G

61735443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233827-G-T

61735751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10233551-G-T

61735787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 10233515-G-T

http://identifiers.org/hco/11/GRCh38#61735822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10233480-C-A

61735822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233480-C-T

61735829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233474-A-G

http://identifiers.org/hco/11/GRCh38#61735844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10233459-C-A

61735844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233459-C-T

61735855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233448-T-C

61736041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233298-G-A

61736122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233212-G-T

http://identifiers.org/hco/11/GRCh38#61736140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10233191-A-C

61736140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233191-A-G

61736140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233191-A-T

61736182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233163-G-A

61736182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233163-G-T

http://identifiers.org/hco/11/GRCh38#61736257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10233115-C-A

61736260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233112-G-C

61736260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10233112-G-T

61736262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 10233110-C-T

61736422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10232993-G-A

61736430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10232985-A-G

61736633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10232805-A-G

61736891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10232583-A-G

http://identifiers.org/hco/11/GRCh38#61737030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10232442-A-C

61737030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10232442-A-G

61737376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10232117-G-A

61737376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10232117-G-T

61737550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10231255-A-G

http://identifiers.org/hco/11/GRCh38#61737846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10231005-A-C

61737869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230982-G-A

61737869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230982-G-T

61737895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230956-T-C

61737895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230956-T-G

http://identifiers.org/hco/11/GRCh38#61737900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10230951-C-A

61737900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230951-C-T

http://identifiers.org/hco/11/GRCh38#61738217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10230682-C-A

61738217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230682-C-G

61738217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230682-C-T

61738248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230652-T-A

http://identifiers.org/hco/11/GRCh38#61738265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10230635-C-A

61738265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10230635-C-T

61738394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230535-C-T

61738561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230383-G-A

61738697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230267-G-A

61738727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230207-G-A

61738732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10230200-G-A

61739716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10229339-T-G

61739727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10229326-G-A

61739734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10229317-T-G

61739787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10229221-G-C

61739787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10229221-G-T

61739933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10229025-C-T

61740159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228820-G-A

http://identifiers.org/hco/11/GRCh38#61740347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10228637-C-A

61740381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228607-G-T

61740470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 10228551-G-T

61740608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228418-G-A

61740655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228409-G-A

61740655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228409-G-T

http://identifiers.org/hco/11/GRCh38#61740686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10228371-C-A

61740686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228371-C-T

61740707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228349-A-G

61740971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228057-G-A

61741027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228024-A-G

61741027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228024-A-T

http://identifiers.org/hco/11/GRCh38#61741044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10228008-C-A

61741044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10228008-C-T

61741105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10227957-C-G

61741105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10227957-C-T

http://identifiers.org/hco/11/GRCh38#61741255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10227825-A-C

http://identifiers.org/hco/11/GRCh38#61741261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10227819-C-A

61741388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10227692-T-C

61742168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10227283-C-G

61742426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10227083-T-C

61742639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 10226889-T-C

61742989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226644-A-G

61743090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226541-C-T

http://identifiers.org/hco/11/GRCh38#61743404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10226102-A-C

61743413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226092-A-G

61743413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226092-A-T

61743488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226028-T-C

http://identifiers.org/hco/11/GRCh38#61743517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10226001-C-A

61743517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226001-C-T

http://identifiers.org/hco/11/GRCh38#61743518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10226000-C-A

61743518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 10226000-C-T

61744519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224996-G-A

61744519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224996-G-C

61744519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224996-G-T

61744550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224965-T-C

61744625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224888-G-A

61744706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224826-G-T

61744866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224670-G-A

61744866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224670-G-T

61744906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224621-T-A

61744906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224621-T-C

61744917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224610-G-T

61745100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224417-G-T

61745368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224162-G-A

61745368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224162-G-T

http://identifiers.org/hco/11/GRCh38#61745392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10224140-C-A

61745392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224140-C-T

http://identifiers.org/hco/11/GRCh38#61745481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10224058-C-A

61745481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10224058-C-T

http://identifiers.org/hco/11/GRCh38#61745512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10224036-C-A

61745674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223876-G-A

61745674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223876-G-T

61745826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223708-T-C

61745893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223660-G-A

61745893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223660-G-T

61746070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223545-A-G

61746163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223471-C-T

http://identifiers.org/hco/11/GRCh38#61746258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#10223370-C-A

61746258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 10223370-C-T

http://identifiers.org/hco/11/GRCh38#61746571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#10223055-C-A

61746571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10223055-C-G

61746706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10222933-A-G

61746767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10222860-G-T

61746772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10222855-G-T

61746773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10222854-G-A

61746806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10222820-G-A

61746806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1165
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 10222820-G-T