http://identifiers.org/hco/11/GRCh38#87037994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88987847-C-A

87037994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88987847-C-T

87038773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88987172-G-A

87038938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88987049-A-G

http://identifiers.org/hco/11/GRCh38#87039410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88986576-A-C

87039410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88986576-A-G

87039711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88986288-C-T

87039827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88986056-C-T

87040093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88985835-T-G

87041085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88985259-C-T

87041122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88985225-A-G

87041700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88984743-A-G

87041789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88984671-A-G

87041839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88984623-T-A

87041938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88984519-C-T

87044212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88976877-T-C

87044228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88976855-G-C

87044600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88976389-A-G

87045409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88976201-C-T

87045522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88976100-C-T

87054799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88975698-T-A

87054841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88975656-G-T

87054873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88975626-G-A

87054873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88975626-G-C

87054881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88975618-C-T

87054896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88975594-G-A

87056497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88974396-T-G

87056740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88974102-G-T

87056852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88974000-A-G

87056960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973913-G-T

87057013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973882-C-T

87057192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973711-T-G

87057287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973620-A-G

87057385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973386-T-C

http://identifiers.org/hco/11/GRCh38#87057433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88973312-A-C

87057507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973233-T-C

http://identifiers.org/hco/11/GRCh38#87057546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88973190-A-C

87057546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88973190-A-G

87061410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88964213-G-A

87061416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88964207-A-G

87061475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88964161-A-G

87061584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88964061-A-G

87061666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963981-C-T

87061691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963950-A-G

87061693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963948-G-T

87061818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963823-T-C

http://identifiers.org/hco/11/GRCh38#87062088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88963628-C-A

87062088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963628-C-T

87062165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963560-C-T

87062347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963344-G-A

87062375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88963316-G-T

87063399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88962377-G-T

87063582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88962206-T-C

87063826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961967-A-G

http://identifiers.org/hco/11/GRCh38#87063910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88961880-A-C

87064124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961798-T-C

87064183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961745-A-G

87064291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961671-A-G

87064428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961543-A-T

87064455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88961516-C-T

87066256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957725-T-A

87066270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957711-A-G

87066313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957676-C-T

87066584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957405-T-A

87066587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957402-T-A

87066592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957397-G-A

87066592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957397-G-T

87066618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957374-G-A

87066618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957374-G-C

87066618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957374-G-T

http://identifiers.org/hco/11/GRCh38#87066624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88957368-C-A

87066624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957368-C-T

87066717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957279-G-A

87066771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957241-A-T

87066773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88957239-T-C

87067549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956615-T-C

http://identifiers.org/hco/11/GRCh38#87067579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88956585-C-A

87067579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956585-C-T

87067623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956542-G-A

87067623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956542-G-C

87067661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88956503-T-C

87067879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88955878-A-G

87067879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88955878-A-T

87067957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88955804-T-A

87068084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88955685-T-A

87068149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88955625-C-T

87070627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88954618-C-T

87071437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88954065-A-G

87071496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88954006-T-C

87071686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88953820-T-G

http://identifiers.org/hco/11/GRCh38#87071694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88953812-C-A

87071694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88953812-C-T

http://identifiers.org/hco/11/GRCh38#87071772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88953731-A-C

87071772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88953731-A-G

87071801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88953695-C-G

87081252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88938856-T-C

87081627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88938548-C-T

87082517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88935894-A-T

87082780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88935697-G-C

87083123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88935354-T-A

87083284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88935193-T-A

87083307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88935171-G-C

87083438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88935044-T-C

87083645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88934876-A-T

87083763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88934769-A-G

87084057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88934505-G-A

87090235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88930409-A-G

87090235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88930409-A-T

http://identifiers.org/hco/11/GRCh38#87090239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88930405-A-C

87090568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88930061-A-T

87090879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88929785-T-C

87091064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88929560-T-C

87091339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88929229-C-T

87091453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88929111-A-T

87091490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88929030-G-A

87091490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88929030-G-T

87091523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928998-T-A

87091523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928998-T-C

87091523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928998-T-G

http://identifiers.org/hco/11/GRCh38#87091545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88928971-C-A

87091545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928971-C-G

87091625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928893-C-T

87091761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928768-T-A

87091761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88928768-T-G

87097783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88919175-T-A

87097878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88919079-G-A

http://identifiers.org/hco/11/GRCh38#87100975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88918249-C-A

87101047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88918190-T-C

87101294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88917976-A-G

87101421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88917852-T-A

87101532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88917620-C-G

87111000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88913881-C-T

87111022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88913859-T-A

87111097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88913804-A-G

87111930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88913329-C-T

87112064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88913213-T-C

http://identifiers.org/hco/11/GRCh38#87112202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88913077-C-A

87112232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88913045-T-G

87112475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912836-G-T

87112712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912621-G-T

87112783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912556-T-C

87113090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88912265-A-G

http://identifiers.org/hco/11/GRCh38#87113357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88912011-A-C

87113399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88911988-A-T

http://identifiers.org/hco/11/GRCh38#87113407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88911980-A-C

87113407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88911980-A-G

87113567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88911899-G-A

87113884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88911551-G-A

http://identifiers.org/hco/11/GRCh38#87115765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88908957-C-A

87115868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88908870-G-T

87115972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88908616-A-G

87116031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88908551-A-G

http://identifiers.org/hco/11/GRCh38#87116151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88908443-A-C

87116257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88908335-G-A

87122334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88907763-A-T

87125650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905673-G-A

87125694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905636-T-C

87125762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905570-T-C

87125766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905566-C-G

87125785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905543-G-A

87125879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905450-T-A

http://identifiers.org/hco/11/GRCh38#87125935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88905391-A-C

87126108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905160-G-A

87126155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88905031-G-A

87126195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904930-A-G

87126251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904874-C-G

87126251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904874-C-T

87126497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904685-T-A

87126497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904685-T-C

87126573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904606-G-A

87126573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904606-G-T

87126613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904514-A-G

87126833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904303-T-C

87126848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904288-C-G

87126864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904272-A-G

87126959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904189-T-C

http://identifiers.org/hco/11/GRCh38#87127108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88904098-C-A

87127108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88904098-C-G

87127214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903998-A-G

87127222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88903990-G-A

http://identifiers.org/hco/11/GRCh38#87127296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88903923-A-C

87137871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901613-G-C

87137893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901591-T-C

http://identifiers.org/hco/11/GRCh38#87138075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88901411-A-C

87138075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901411-A-G

87138685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901249-T-G

87138687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88901247-G-C

87139860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88898421-G-A

87148138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88898031-C-T

87148333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897840-C-T

87148372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897801-C-G

87148642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897555-A-T

87148768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88897431-G-C

87149304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88896906-A-G

87149603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88896638-T-C

87157249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88893275-T-C

87157303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88893233-A-T

87157322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88893211-T-C

http://identifiers.org/hco/11/GRCh38#87157358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88893175-C-A

87157358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88893175-C-G

87157360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88893173-G-A

87157426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88893112-A-G

http://identifiers.org/hco/11/GRCh38#87157435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88893103-A-C

87157435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88893103-A-T

87157444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88893079-T-C

87157469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88893053-A-G

http://identifiers.org/hco/11/GRCh38#87157524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88893006-A-C

87157524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88893006-A-G

87157524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88893006-A-T

http://identifiers.org/hco/11/GRCh38#87157541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88892962-C-A

87157549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88892954-A-G

87157575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88892930-G-T

http://identifiers.org/hco/11/GRCh38#87157644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88892850-C-A

87157644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88892850-C-T

87157741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88892708-A-G

87157782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88892670-G-T

87157818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 88892652-G-T

87157941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892519-G-A

87157941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892519-G-C

87157941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892519-G-T

87157959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892503-T-A

http://identifiers.org/hco/11/GRCh38#87157995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88892476-C-A

87157995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88892476-C-T

http://identifiers.org/hco/11/GRCh38#87160392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88891629-C-A

87160546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891474-T-G

87160762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88891279-A-G

87161718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890861-T-C

87161744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890827-T-A

87162019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88890561-A-G

87173179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88886124-A-G

87173209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88886100-G-A

87173396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885935-T-C

87174032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885411-A-G

87174083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885371-A-G

87174224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885235-C-T

87174363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88885108-A-G

87175127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88884566-G-A

87175948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88883687-T-A

87176762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88883312-T-C

87176927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88883156-T-C

87177420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88882734-A-T

http://identifiers.org/hco/11/GRCh38#87184774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88874396-A-C

87184776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88874394-A-G

87184868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88874316-T-C

87185302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88873722-G-A

87185302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88873722-G-C

87187150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872405-G-A

87187184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872376-T-C

87187219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872340-T-C

87187242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872317-G-A

87187280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872279-G-A

87187450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872124-A-G

87187532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88872031-A-G

87187635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871919-G-A

http://identifiers.org/hco/11/GRCh38#87187909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88871634-C-A

87187966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871565-A-T

87187985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871546-T-G

87188147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871401-T-G

87188184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871368-T-C

87188196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871358-T-C

87188257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88871293-G-A

87190002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88867631-A-G

http://identifiers.org/hco/11/GRCh38#87190256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88867377-C-A

87193972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866329-T-G

87193986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866315-A-G

87194199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88866115-A-G

87195941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88864652-A-G

87196180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88864473-A-T

87196243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88864410-C-T

http://identifiers.org/hco/11/GRCh38#87196385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88864303-A-C

87196461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88864220-T-G

87196591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88864069-T-C

87196764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863807-A-G

87197054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863540-T-C

87197268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863464-A-G

87197305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863423-A-G

87197311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863417-T-C

http://identifiers.org/hco/11/GRCh38#87197527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88863243-C-A

87197529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863241-A-G

87197581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863182-T-G

87197614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863160-A-G

87197614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88863160-A-T

87197820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88862973-T-G

87197879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88862912-T-C

http://identifiers.org/hco/11/GRCh38#87197904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88862887-A-C

87197911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88862881-T-C

87198910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88862177-C-T

87198963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88862125-T-A

http://identifiers.org/hco/11/GRCh38#87198966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88862122-A-C

87199009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88862084-G-A

87199317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859893-T-A

87199658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859683-G-A

87200090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859463-C-G

87200110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859443-A-G

87200119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859434-T-G

87200249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859322-G-T

87200378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88859197-T-C

87205452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858731-T-C

87205531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858658-A-G

http://identifiers.org/hco/11/GRCh38#87205598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88858517-C-A

87205598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858517-C-G

87205598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858517-C-T

87205806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858318-T-C

87205824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858268-C-T

87205871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858211-G-A

87205981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858133-T-G

87206120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88858010-T-C

87206440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88857754-G-A

87206445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88857749-T-C

87206447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88857747-T-C

87206626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88857578-T-A

87216698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88855947-T-C

87217090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88855606-G-T

87217161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88855371-A-G

87217191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88855350-G-T

87217812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88854670-T-G

87218094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88854356-G-C

87218128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88854315-G-A

87218139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88854305-A-G

87219657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88853571-C-G

87219782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88853360-G-A

87220257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852909-A-G

87220411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852762-T-G

87220552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852622-G-A

87220552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852622-G-C

87220597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852578-T-C

87220738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852377-A-G

87220792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88852330-G-A

http://identifiers.org/hco/11/GRCh38#87221209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88850799-C-A

87221209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88850799-C-T

87221309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88850702-A-G

http://identifiers.org/hco/11/GRCh38#87221615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88850428-A-C

87229984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88849852-C-T

87231359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88848442-T-C

87231361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88848440-T-G

87231711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88848101-T-C

87236540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845470-T-C

87236544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845466-A-G

87236544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845466-A-T

http://identifiers.org/hco/11/GRCh38#87236580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88845426-C-A

87236585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845421-A-G

87236752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845267-G-A

87236752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845267-G-C

87236752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845267-G-T

87236757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845262-T-A

87236763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88845256-A-T

87237404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88844008-A-G

87237462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88843965-A-T

87239077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88843001-A-G

87239154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842924-T-C

http://identifiers.org/hco/11/GRCh38#87239170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88842906-A-C

87239328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842746-A-G

87239329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842745-C-T

87239405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842676-T-C

87239407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842674-T-C

http://identifiers.org/hco/11/GRCh38#87239834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88842279-A-C

87239834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842279-A-G

87239952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88842165-T-A

87240266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88841886-G-T

87240455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88841648-T-C

http://identifiers.org/hco/11/GRCh38#87240462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88841641-A-C

87240462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88841641-A-G

87240540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88841488-A-T

87240781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88841266-T-C

87240785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88841262-T-C

87260239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88840561-G-A

87264592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88840213-T-C

87265158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88833253-A-G

http://identifiers.org/hco/11/GRCh38#87265453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88832966-A-C

87265524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88832932-G-A

87265524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88832932-G-C

87265729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88832747-C-G

87265824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88832659-A-G

87273853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88828439-G-A

87273878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88828414-T-G

87273896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88828404-G-C

87274098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88828227-G-T

87274293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88828062-G-C

87274411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827942-T-C

87274548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827793-G-A

87275357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827316-A-G

87275368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827308-G-A

87275373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827303-C-T

87275410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827266-C-T

http://identifiers.org/hco/11/GRCh38#87275437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88827253-C-A

87275630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88827081-A-G

http://identifiers.org/hco/11/GRCh38#87278879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88824376-C-A

87278962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88824293-T-C

87279068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88824203-T-C

87279185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88824107-T-C

87279407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823919-C-T

87279449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823874-A-G

87279668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823714-T-G

http://identifiers.org/hco/11/GRCh38#87279722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88823654-C-A

87279722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823654-C-T

87279809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823585-T-C

87279815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823579-C-G

87280052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823396-G-T

87280086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823341-A-G

87280145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823267-C-T

87280250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823164-T-G

87280377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88823080-G-T

87280602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822894-T-C

87280720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822773-G-A

87280776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822731-T-C

87280797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822711-C-T

87280888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822618-A-T

87280966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822546-A-T

87281130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88822407-A-G

87281538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88821980-G-A

87281538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88821980-G-T

87281619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88821895-A-G

87281620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88821894-T-C

87282150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88821345-G-T

87284134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88820678-G-T

http://identifiers.org/hco/11/GRCh38#87284616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88820241-A-C

87284862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88820015-C-G

87284870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88820007-A-G

87285030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88819612-G-C

87285208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88819452-C-T

87286714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88819083-G-A

87290235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88818229-A-G

http://identifiers.org/hco/11/GRCh38#87290524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88817976-A-C

87290618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88817859-A-G

87290879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88817618-A-T

87290943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88817554-G-T

87291088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88817435-T-C

87291467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88817118-C-T

87291576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88817091-G-T

87291993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816914-T-C

87292191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816752-A-G

87292216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816736-C-T

87292290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816693-A-G

87292662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88816243-A-G

87292938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88815983-T-C

87293151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88815769-A-G

87293306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88815620-T-C

87294911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88815173-T-G

87294966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88815119-A-G

87295404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814719-T-G

87295487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814637-G-A

87295722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814429-G-A

87295722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814429-G-C

87295722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814429-G-T

87295724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814427-A-G

87295761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814390-T-A

87295762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814389-G-A

87295762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814389-G-T

87295880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814270-A-T

87295900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814250-G-A

87295928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814222-T-C

87295944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814206-A-G

87295944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814206-A-T

87296166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88814146-T-C

87296370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88813969-C-T

87296489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88813873-A-G

87296521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88813842-G-A

87296821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88813639-G-C

87296957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88813582-C-T

http://identifiers.org/hco/11/GRCh38#87297075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88813462-A-C

87297569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812992-C-T

87297715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812852-A-G

87297903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812414-A-G

87297904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812413-T-A

87297910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812407-A-G

87297910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812407-A-T

87298106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812184-C-T

87298145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812148-A-G

87298252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88812036-C-T

87298381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811890-T-C

http://identifiers.org/hco/11/GRCh38#87298428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88811848-A-C

87299553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811730-A-G

87299663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811622-T-C

87299697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811599-G-A

87299808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811494-G-A

87299808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811494-G-T

87299998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811290-T-C

http://identifiers.org/hco/11/GRCh38#87300301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88811063-C-A

87300301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88811063-C-T

87300565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810625-T-A

87300812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810335-C-T

87300838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810309-A-G

87300847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810300-T-A

87300847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810300-T-C

87300872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810276-G-A

87300926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810223-T-C

87300927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810222-G-C

87301024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88810139-C-T

87301621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809832-C-T

87301640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88809813-T-C

87302035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808421-T-C

87302035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808421-T-G

87302165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808337-A-G

87302278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808239-T-C

87302390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88808127-A-G

87302422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88808095-C-G

87302423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88808094-A-G

http://identifiers.org/hco/11/GRCh38#87302470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88808048-C-A

87302470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808048-C-T

http://identifiers.org/hco/11/GRCh38#87302503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88808016-C-A

87302503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88808016-C-T

http://identifiers.org/hco/11/GRCh38#87302531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88807992-C-A

87302531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807992-C-G

http://identifiers.org/hco/11/GRCh38#87302552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88807965-C-A

http://identifiers.org/hco/11/GRCh38#87302571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88807946-A-C

87302580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807938-A-G

http://identifiers.org/hco/11/GRCh38#87302585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88807933-C-A

87302585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807933-C-T

87302660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807859-G-A

87302840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807694-A-G

87302872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88807662-G-T

87304478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806794-A-G

87304496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806776-C-G

87304732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88806577-C-T

87305384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805946-A-G

http://identifiers.org/hco/11/GRCh38#87305864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88805763-C-A

http://identifiers.org/hco/11/GRCh38#87306019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88805619-A-C

87306019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805619-A-G

http://identifiers.org/hco/11/GRCh38#87306098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88805539-A-C

87306098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805539-A-G

87306102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805535-G-A

87306102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805535-G-T

87307120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88805196-C-T

87307593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88804804-A-G

87307593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88804804-A-T

87307754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88804535-C-G

87307812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88804480-A-G

87307927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88804372-G-C

87308389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88803956-A-G

87308450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88803899-T-A

87308450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88803899-T-C

87309592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88803314-T-C

87309810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88802850-A-G

87310290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88802386-C-T

87311955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88802223-C-T

87312270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88801888-A-G

87312645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88801551-T-G

87313142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800922-A-G

http://identifiers.org/hco/11/GRCh38#87313395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88800713-C-A

87313408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800700-A-G

http://identifiers.org/hco/11/GRCh38#87313621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88800497-C-A

87314088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88800106-T-A

87314554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 88797169-G-A

87314563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88797160-G-A

http://identifiers.org/hco/11/GRCh38#87314599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88797124-C-A

87314809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796959-C-T

http://identifiers.org/hco/11/GRCh38#87314827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88796941-C-A

87314827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796941-C-T

87314891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796906-T-C

87314973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796853-A-G

87315030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796791-T-A

87316899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796175-G-A

87316899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796175-G-T

87316992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796084-A-G

87317014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88796062-C-T

http://identifiers.org/hco/11/GRCh38#87317426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88795353-A-C

87317596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88795178-G-A

87318004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794104-A-T

http://identifiers.org/hco/11/GRCh38#87318044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88794066-C-A

87318044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794066-C-T

87318049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794061-A-G

87318098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88794004-T-G

87318249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88793849-T-C

http://identifiers.org/hco/11/GRCh38#87319334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88793030-A-C

87319416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792921-G-A

87319416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792921-G-T

87319666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792675-T-C

87319806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792568-T-A

87319865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792516-G-C

87320000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792402-G-A

87320000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88792402-G-T

87320712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791633-C-T

87320765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791581-A-G

87320802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791544-T-A

87320946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791401-A-G

87321097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791278-G-C

87321097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791278-G-T

87321100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791275-T-C

http://identifiers.org/hco/11/GRCh38#87321132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88791243-C-A

87321132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88791243-C-T

87321554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790834-T-C

87321603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790784-G-A

87321778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790615-T-A

87321809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790584-A-G

87321854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790555-G-A

87321904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790508-A-G

87321977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790430-T-C

87321977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790430-T-G

87322176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790227-G-A

87322176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790227-G-T

http://identifiers.org/hco/11/GRCh38#87322177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88790226-A-C

87322204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88790200-T-C

87322550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789892-G-T

87322622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789815-G-C

87322773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789671-A-G

87322829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789615-C-G

87322829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789615-C-T

http://identifiers.org/hco/11/GRCh38#87322839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88789605-A-C

87322839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789605-A-G

http://identifiers.org/hco/11/GRCh38#87322841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88789603-A-C

87323086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789342-G-C

87323086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789342-G-T

87323242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789192-A-G

http://identifiers.org/hco/11/GRCh38#87323328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88789104-C-A

87323328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88789104-C-T

87323454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788993-A-G

87323533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788897-T-C

http://identifiers.org/hco/11/GRCh38#87323653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88788780-C-A

87323653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788780-C-T

87323687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788751-C-T

87323782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788670-T-A

87323782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788670-T-C

http://identifiers.org/hco/11/GRCh38#87323810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88788650-C-A

87323874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788586-T-G

87325499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88788306-T-C

http://identifiers.org/hco/11/GRCh38#87325795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88787906-C-A

http://identifiers.org/hco/11/GRCh38#87325834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88787878-C-A

87325879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787799-T-A

87325902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787777-C-G

87325902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787777-C-T

87326193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787620-G-A

87326354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787487-C-T

87326386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787455-G-T

http://identifiers.org/hco/11/GRCh38#87326418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88787424-C-A

87326554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88787307-A-G

87326777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88786367-T-A

87326790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88786354-T-G

http://identifiers.org/hco/11/GRCh38#87326871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88786285-A-C

87326948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88786227-T-A

87326986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88786203-T-C

87327056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88786124-G-T

87327155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88786035-T-C

http://identifiers.org/hco/11/GRCh38#87327182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#88786008-A-C

87327200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88785990-G-T

87327418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88785774-C-G

87328138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26167
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 88785692-T-C