90773485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106652618-A-G

90773552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106652857-T-C

90774219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106653647-A-G

90774344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106653772-A-G

http://identifiers.org/hco/1/GRCh38#90774386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106653814-A-C

90774756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106654187-G-A

90775002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106654437-A-G

90776056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106654973-G-A

90776056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106654973-G-C

90776099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106655014-C-T

http://identifiers.org/hco/1/GRCh38#90776323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106655219-C-A

90776453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106655368-G-A

90776542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106655403-T-C

90776866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106655676-T-C

90777114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106655921-T-A

90777114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106655921-T-C

90777401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656230-C-T

90778391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656691-A-T

90778784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106657064-G-T

90778844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106657126-A-G

http://identifiers.org/hco/1/GRCh38#90778882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106657165-C-A

90778985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106657259-C-T

90780581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106658694-G-C

90780701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106658769-A-G

http://identifiers.org/hco/1/GRCh38#90780715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106658786-A-C

http://identifiers.org/hco/1/GRCh38#90780720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106658793-C-A

90780720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106658793-C-T

http://identifiers.org/hco/1/GRCh38#90781200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106659236-A-C

90781338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106659364-G-A

90781389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106659418-G-C

90781692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106659713-G-C

http://identifiers.org/hco/1/GRCh38#90781951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106660471-A-C

90782178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106660687-C-T

http://identifiers.org/hco/1/GRCh38#90782353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106660862-A-C

90782353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106660862-A-G

90783744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106662590-G-A

90783744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106662590-G-T

90783977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106662800-G-T

90784071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106662889-T-C

90784305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106663241-C-G

90785266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665039-T-A

90785307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665077-G-A

90785318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665096-G-A

90785673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665406-G-C

90785737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665468-A-T

90785771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665502-G-A

90786052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665778-A-G

90786092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665812-C-T

90786205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665909-C-G

90786205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106665909-C-T

90786566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106666304-G-A

http://identifiers.org/hco/1/GRCh38#90786593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106666331-A-C

90786792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106666597-C-T

http://identifiers.org/hco/1/GRCh38#90786929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106666740-A-C

90787152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106666889-T-G

90787494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106667205-G-A

90787537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106667249-C-T

http://identifiers.org/hco/1/GRCh38#90792726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106668983-A-C

90792726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106668983-A-T

90793026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669313-G-A

90793822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669917-G-A

90793830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669925-A-G

90793962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670041-C-T

90793990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670049-T-C

http://identifiers.org/hco/1/GRCh38#90794054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106670095-C-A

90794068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670110-G-A

90794072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670114-G-A

http://identifiers.org/hco/1/GRCh38#90794662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106670729-A-C

90794744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670814-A-G

90794774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670843-T-C

90794850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670918-C-T

90795186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671258-C-T

90795396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671418-C-T

90795488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671511-C-G

90795661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671670-G-A

90795661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671670-G-T

90795865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671866-A-G

90795943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106672105-A-G

90795976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106672136-A-T

90796370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673425-A-G

http://identifiers.org/hco/1/GRCh38#90796804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106673825-C-A

http://identifiers.org/hco/1/GRCh38#90796843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106673875-C-A

90797167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674176-C-G

90797190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674202-G-A

90797203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674215-A-G

90797612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674961-T-C

90798889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675071-C-G

90798935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675113-T-C

90798977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675150-C-T

90799007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675176-C-T

90799053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675219-G-C

90799473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675623-G-A

90799531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675685-C-T

90799602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675755-G-T

90799833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106675977-G-A

90799984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676113-T-C

90800106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676234-C-T

90800192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676307-T-A

90800389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676498-G-C

http://identifiers.org/hco/1/GRCh38#90800718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106676832-C-A

90800718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676832-C-T

90800765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676871-A-G

90800811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676915-G-A

90801361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677733-A-G

90801502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677859-G-A

90801557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677905-A-T

90801627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677974-G-A

http://identifiers.org/hco/1/GRCh38#90801735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106678137-A-C

90801846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678340-G-A

90807290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683261-G-C

90807315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683286-G-A

90807381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683352-T-C

http://identifiers.org/hco/1/GRCh38#90807470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106683418-C-A

90807470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683418-C-T

90807900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106684247-A-T

90808020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106684284-G-T

90808096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106684337-T-C

90808101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106684342-C-G

90808175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684401-G-A

90808280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684502-A-G

90808852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684715-T-C

90808879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684742-A-T

90809277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106685138-A-G

90809467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685342-C-T

90809468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685343-G-A

90809468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685343-G-C

90809499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685367-T-C

http://identifiers.org/hco/1/GRCh38#90809821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106685709-C-A

90809846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685734-A-G

90809870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685757-G-A

90810026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106685880-T-C

90810126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106686200-A-G

90810137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106686289-C-G

90810137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106686289-C-T

90810260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106686412-A-G

90811844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106688394-T-C

90811948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106688467-G-A

90812008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106688519-T-A

90812008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106688519-T-C

90813859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106689398-T-C

90813961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106689512-T-C

90813965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106689516-G-A

90814007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106689557-G-T

http://identifiers.org/hco/1/GRCh38#90814907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106690456-C-A

90814907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106690456-C-T

90815301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106690841-G-A

http://identifiers.org/hco/1/GRCh38#90815488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106690992-C-A

90815488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106690992-C-T

90815548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106691053-A-G

90815559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106691064-C-T

90815707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106691198-G-A

90818846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106692037-C-T

90818869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106692060-T-C

90818919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106692107-G-T

90819006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106692169-G-A

90819006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106692169-G-T

90819080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106692240-C-T

90820340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106694321-C-T

90820460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106694437-G-A

90820463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106694440-T-C

http://identifiers.org/hco/1/GRCh38#90820677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106694648-C-A

90820677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106694648-C-T

90821170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106695150-G-A

90821593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106695537-C-G

90821595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106695539-G-A

90821809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106695737-C-T

90821823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106695751-A-G

http://identifiers.org/hco/1/GRCh38#90821843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106695771-A-C

90821890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106695815-A-T

90822091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106695974-T-C

90822415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106696293-T-C

90823101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106696425-G-A

90823301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106696597-T-C

90823564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106696811-T-G

90823795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106697220-G-A

90824611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106698208-T-C

90824621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106698218-A-T

90824752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106698306-A-T

90824897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106698436-C-T

90825296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106698768-G-A

90826982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106700026-T-C

90827042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106700086-A-T

90827060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106700105-T-C

90827725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106700772-G-T

90827760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106700805-C-T

90827841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106700907-G-A

90828161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106701537-G-A

90828348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106701925-G-A

90828348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106701925-G-T

90828621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106702387-G-A

90828767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106702539-C-T

http://identifiers.org/hco/1/GRCh38#90828940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106702712-C-A

90829305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106703089-C-G

90829322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106703106-T-A

90829322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106703106-T-C

90829744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106703462-G-A

90829990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106703705-C-T

http://identifiers.org/hco/1/GRCh38#90830391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106704103-C-A

90830463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106704189-G-T

90830484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106704210-A-G

90830640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106704353-T-C

90830802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106704493-G-A

90831018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106704698-T-C

http://identifiers.org/hco/1/GRCh38#90831106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106704959-C-A

90831497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705300-G-A

90831554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705344-G-T

90831594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705379-G-A

90831594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705379-G-T

90831674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705451-C-T

90831695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705473-G-T

90832017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705743-T-C

http://identifiers.org/hco/1/GRCh38#90832022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106705748-C-A

90832022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106705748-C-T

http://identifiers.org/hco/1/GRCh38#90832907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106706500-A-C

90832917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106706510-C-T

http://identifiers.org/hco/1/GRCh38#90833790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106707392-A-C

90834208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106707808-C-T

90834260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106707859-T-C

90836212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709344-G-A

90836239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709366-G-A

90836239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709366-G-T

90836248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709375-G-A

http://identifiers.org/hco/1/GRCh38#90836277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106709403-C-A

90836277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709403-C-G

90836277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709403-C-T

90836297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106709414-C-T

90837313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710358-C-T

90837547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710546-T-C

90837556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710555-C-T

90837614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710613-G-A

90837614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710613-G-T

90837656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710655-G-T

90837690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710688-G-C

90837724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710707-G-A

http://identifiers.org/hco/1/GRCh38#90837753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106710734-C-A

90837753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710734-C-G

90837753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106710734-C-T

90837929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106710902-A-T

90838004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106710975-T-C

90838669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106711235-T-C

90839527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106711767-G-C

90839570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106711813-T-C

90839633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106711878-T-C

90839639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106711884-T-C

90839706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106711930-C-T

90839921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106712093-T-A

http://identifiers.org/hco/1/GRCh38#90841513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106713785-C-A

90841520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106713792-C-T

http://identifiers.org/hco/1/GRCh38#90841675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106713903-C-A

90841675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106713903-C-T

90841698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106713925-C-T

http://identifiers.org/hco/1/GRCh38#90841791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106714021-A-C

90841915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106714144-G-A

90842172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106714403-G-A

90842538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106714721-T-C

90842620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106714798-C-T

http://identifiers.org/hco/1/GRCh38#90842714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106714853-C-A

90842714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106714853-C-T

90843059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106715175-T-G

90843180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106715292-A-G

90843672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106715747-G-C

90843709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106715782-G-A

90844030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716067-C-T

90844638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716327-G-A

90844665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716352-C-T

90844720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716413-T-G

90844850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716498-C-G

90845065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716696-A-G

http://identifiers.org/hco/1/GRCh38#90845127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106716758-A-C

90845127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106716758-A-T

90845768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106717817-G-C

90846104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106718148-C-T

90846147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106718191-C-T

http://identifiers.org/hco/1/GRCh38#90847723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106718938-C-A

90847793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106719003-A-G

90847971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106719576-T-C

90848524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106720062-G-T

90849486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106720807-T-C

90849494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106720815-T-A

90849890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106721165-T-A

http://identifiers.org/hco/1/GRCh38#90850155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106721417-A-C

90850501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106721763-G-A

90850904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106722142-G-A

http://identifiers.org/hco/1/GRCh38#90850940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106722166-A-C

90850940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106722166-A-G

90851473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106722444-A-G

90851579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106722523-G-A

90851579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106722523-G-T

90851647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106722567-G-A

90851647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27140
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106722567-G-C