http://identifiers.org/hco/13/GRCh38#18946808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48961169-C-A

18946808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961169-C-G

18946808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961169-C-T

http://identifiers.org/hco/13/GRCh38#18946833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48961191-C-A

18946833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961191-C-T

18946889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961247-G-A

18946889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961247-G-C

18946889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961247-G-T

http://identifiers.org/hco/13/GRCh38#18946907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48961265-C-A

18946907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48961265-C-T

18947026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48961387-A-G

18947026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48961387-A-T

18947043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48961403-G-T

18947744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962157-A-G

http://identifiers.org/hco/13/GRCh38#18947793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48962216-C-A

18947793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962216-C-G

18947809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962232-G-A

18947907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962418-T-C

18947961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962476-A-G

http://identifiers.org/hco/13/GRCh38#18947985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48962509-C-A

18948181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962715-G-A

18948364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48962895-C-T

http://identifiers.org/hco/13/GRCh38#18948671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48963150-C-A

18948671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48963150-C-G

18949653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964397-T-C

http://identifiers.org/hco/13/GRCh38#18949907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48964654-C-A

18949907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964654-C-T

18949908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964655-G-A

18949908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964655-G-T

18949956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964704-C-T

18949971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964723-C-G

18949971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964723-C-T

18949989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964737-A-T

18950010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964764-G-C

18950178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48964880-T-G

18950335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965036-G-C

18950378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965084-G-A

18950423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965149-C-G

18950423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965149-C-T

18950611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965276-T-C

http://identifiers.org/hco/13/GRCh38#18950715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48965378-A-C

18950792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965434-G-A

18950856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965489-C-T

18950865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965498-G-A

18950865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965498-G-C

18950983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48965599-G-A

http://identifiers.org/hco/13/GRCh38#18951600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48966328-C-A

18951600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966328-C-T

18951651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966363-G-A

18951651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966363-G-T

http://identifiers.org/hco/13/GRCh38#18951808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48966522-A-C

18951808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48966522-A-G

18951826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48966540-G-A

18951826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48966540-G-T

http://identifiers.org/hco/13/GRCh38#18951836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48966550-C-A

18951836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48966550-C-G

18951836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48966550-C-T

http://identifiers.org/hco/13/GRCh38#18951855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48966570-C-A

18951855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966570-C-G

18951855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966570-C-T

18951866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966581-G-A

18951866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966581-G-T

18951922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966607-G-T

18951963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966631-T-C

18952036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48966684-C-T

http://identifiers.org/hco/13/GRCh38#18952076-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48966733-A-C

http://identifiers.org/hco/13/GRCh38#18952458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967077-C-A

18952459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967078-A-G

http://identifiers.org/hco/13/GRCh38#18952477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967104-C-A

18952477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967104-C-T

18952493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967130-G-T

18952502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967139-G-A

18952502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967139-G-T

18952507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967150-G-A

18952507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967150-G-C

18952507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967150-G-T

http://identifiers.org/hco/13/GRCh38#18952518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967176-C-A

18952518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967176-C-G

18952518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967176-C-T

http://identifiers.org/hco/13/GRCh38#18952532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967190-C-A

18952532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48967190-C-T

http://identifiers.org/hco/13/GRCh38#18952680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967310-C-A

18952680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967310-C-T

http://identifiers.org/hco/13/GRCh38#18952691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967321-C-A

18952691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967321-C-T

http://identifiers.org/hco/13/GRCh38#18952955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967579-A-C

18952955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967579-A-G

18952955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967579-A-T

18952956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967580-A-G

18953129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967652-C-T

http://identifiers.org/hco/13/GRCh38#18953151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967671-A-C

18953151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967671-A-G

18953167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48967688-A-G

http://identifiers.org/hco/13/GRCh38#18953170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48967690-C-A

http://identifiers.org/hco/13/GRCh38#18953572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48968034-C-A

18953832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48968258-G-A

18953932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48968340-G-T

18953964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48968365-G-A

18953964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48968365-G-T

18954212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48968573-C-G

http://identifiers.org/hco/13/GRCh38#18954278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48968636-C-A

18954781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969221-T-C

http://identifiers.org/hco/13/GRCh38#18954847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969322-A-C

18954847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969322-A-G

18954854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969329-G-A

18954854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969329-G-T

18954868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969343-A-G

18954868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969343-A-T

18954881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969384-T-A

18954970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48969473-T-A

18954970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48969473-T-C

http://identifiers.org/hco/13/GRCh38#18955005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969508-C-A

18955005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48969508-C-T

18955080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969579-A-G

18955080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969579-A-T

http://identifiers.org/hco/13/GRCh38#18955129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969626-C-A

18955129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969626-C-G

18955129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969626-C-T

http://identifiers.org/hco/13/GRCh38#18955146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969643-A-C

18955146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969643-A-G

18955165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969659-T-G

18955292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969753-T-C

18955304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969768-G-C

http://identifiers.org/hco/13/GRCh38#18955394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969853-C-A

18955394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969853-C-G

18955394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969853-C-T

http://identifiers.org/hco/13/GRCh38#18955398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969857-A-C

18955398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969857-A-G

18955398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969857-A-T

18955399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969858-T-A

18955399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969858-T-C

http://identifiers.org/hco/13/GRCh38#18955426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969878-C-A

18955426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969878-C-G

18955426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969878-C-T

18955439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969881-T-A

18955439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969881-T-C

http://identifiers.org/hco/13/GRCh38#18955478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969894-C-A

18955478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48969894-C-T

http://identifiers.org/hco/13/GRCh38#18955582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48969956-A-C

18955694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970072-A-G

18955694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970072-A-T

http://identifiers.org/hco/13/GRCh38#18955722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970101-C-A

18955722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970101-C-G

18955722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970101-C-T

http://identifiers.org/hco/13/GRCh38#18955776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970159-A-C

18955776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970159-A-G

http://identifiers.org/hco/13/GRCh38#18955837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970221-A-C

18955837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970221-A-G

http://identifiers.org/hco/13/GRCh38#18957204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970281-C-A

18957213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970290-G-T

18957303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970356-C-G

18957303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970356-C-T

18957322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970375-A-G

18957454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970470-G-T

18957710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970670-C-G

18957710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970670-C-T

http://identifiers.org/hco/13/GRCh38#18957918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970883-C-A

18957928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970893-A-G

http://identifiers.org/hco/13/GRCh38#18957951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970916-C-A

18957951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970916-C-G

18957951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970916-C-T

http://identifiers.org/hco/13/GRCh38#18957958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970922-C-A

18957958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970922-C-T

http://identifiers.org/hco/13/GRCh38#18957984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48970948-C-A

18957984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970948-C-T

18957995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970959-G-A

18957995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970959-G-C

18957995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48970959-G-T

18958041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48970997-T-A

18958041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48970997-T-C

http://identifiers.org/hco/13/GRCh38#18958185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971132-C-A

18958185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48971132-C-G

18958185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48971132-C-T

18958193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48971140-G-T

18958194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48971141-T-G

http://identifiers.org/hco/13/GRCh38#18958346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971270-C-A

http://identifiers.org/hco/13/GRCh38#18958447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971370-C-A

18958447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971370-C-T

18958768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971618-G-A

18958825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971660-A-G

18958851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971705-A-G

18958851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971705-A-T

18958911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971742-G-A

18958911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971742-G-T

http://identifiers.org/hco/13/GRCh38#18958912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971743-C-A

18958912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971743-C-G

18958912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971743-C-T

18958947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971760-T-C

18958947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971760-T-G

http://identifiers.org/hco/13/GRCh38#18959113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971891-C-A

http://identifiers.org/hco/13/GRCh38#18959175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971948-C-A

18959175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971948-C-T

http://identifiers.org/hco/13/GRCh38#18959188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48971969-A-C

18959195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971976-G-C

18959195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48971976-G-T

18959253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972055-A-G

18959270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972068-G-C

18959270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972068-G-T

18959299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972093-C-T

18959421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972192-A-G

18959495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972280-G-A

http://identifiers.org/hco/13/GRCh38#18959641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48972416-C-A

18959641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972416-C-G

18959641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972416-C-T

18959703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972476-T-C

18959887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972680-C-T

18959895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972688-G-A

18959918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972730-G-A

18959946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48972758-T-C

http://identifiers.org/hco/13/GRCh38#18960193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48972900-C-A

18960193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 48972900-C-G

18960193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 48972900-C-T

18960429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973096-A-G

18960571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973198-A-T

18960647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973271-T-C

http://identifiers.org/hco/13/GRCh38#18961990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973524-C-A

18961990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48973524-C-T

http://identifiers.org/hco/13/GRCh38#18962008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973542-C-A

18962008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48973542-C-G

18962008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48973542-C-T

18962143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973675-A-G

18962190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973719-T-A

18962190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973719-T-C

18962213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973740-A-G

http://identifiers.org/hco/13/GRCh38#18962223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973751-A-C

18962223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973751-A-G

http://identifiers.org/hco/13/GRCh38#18962226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973754-C-A

18962226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973754-C-T

18962373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973863-G-A

18962373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973863-G-C

18962420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973907-A-G

http://identifiers.org/hco/13/GRCh38#18962452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973921-C-A

18962452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973921-C-T

http://identifiers.org/hco/13/GRCh38#18962599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974043-C-A

18962599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48974043-C-T

http://identifiers.org/hco/13/GRCh38#18962617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974061-C-A

18962617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48974061-C-T

18962682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974129-G-A

18962682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974129-G-C

18962682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974129-G-T

http://identifiers.org/hco/13/GRCh38#18962687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974134-C-A

18962687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974134-C-T

http://identifiers.org/hco/13/GRCh38#18962748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974155-C-A

18962748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974155-C-T

18963163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974483-C-T

18963189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974507-G-T

18963292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974601-T-A

18963409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974689-G-A

18963576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974825-G-A

18963576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974825-G-C

http://identifiers.org/hco/13/GRCh38#18963577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974826-C-A

http://identifiers.org/hco/13/GRCh38#18963942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48975000-C-A

18963942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48975000-C-T

18964163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975282-G-A

18964163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975282-G-C

18964163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975282-G-T

18964166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975285-T-A

18964187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975340-T-A

18964187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975340-T-C

18964187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975340-T-G

18964215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975409-T-C

http://identifiers.org/hco/13/GRCh38#18964250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48975455-A-C

18964280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975492-T-G

18964406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975749-G-A

18964567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975930-A-G

http://identifiers.org/hco/13/GRCh38#18964603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48975971-C-A

18964762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976101-T-A

18964861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976168-A-G

http://identifiers.org/hco/13/GRCh38#18965053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976306-C-A

18965053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976306-C-T

18965065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976318-T-C

http://identifiers.org/hco/13/GRCh38#18965138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976396-A-C

18965138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976396-A-G

18965165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976402-G-A

18965165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976402-G-T

18965306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48976545-T-A

18965306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48976545-T-C

18965321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48976566-G-C

18965321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48976566-G-T

http://identifiers.org/hco/13/GRCh38#18965324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976569-C-A

18965324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48976569-C-G

18965324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 48976569-C-T

http://identifiers.org/hco/13/GRCh38#18965398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976645-C-A

18965398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976645-C-G

18965398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976645-C-T

18965497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976748-C-T

18965534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976787-A-G

18965635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976858-G-C

18965639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976862-G-A

18965723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976912-A-G

18965725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976914-C-G

18965806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48977004-G-A

18965806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48977004-G-C

http://identifiers.org/hco/13/GRCh38#19048002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973524-C-A

19048002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48973524-C-T

http://identifiers.org/hco/13/GRCh38#19048020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973542-C-A

19048020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48973542-C-G

19048020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48973542-C-T

19048225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973740-A-G

http://identifiers.org/hco/13/GRCh38#19048235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973751-A-C

http://identifiers.org/hco/13/GRCh38#19048238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973754-C-A

19048238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973754-C-G

19048238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973754-C-T

19048407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973883-T-C

http://identifiers.org/hco/13/GRCh38#19048431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48973907-C-A

19048431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973907-C-G

19048431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973907-C-T

19048464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973921-C-G

19048464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48973921-C-T

http://identifiers.org/hco/13/GRCh38#19048611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974043-C-A

19048611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48974043-C-G

19048611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48974043-C-T

http://identifiers.org/hco/13/GRCh38#19048629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974061-C-A

19048629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48974061-C-G

19048629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48974061-C-T

19048694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974129-G-A

19048694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974129-G-T

http://identifiers.org/hco/13/GRCh38#19048699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974134-C-A

19048699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974134-C-T

http://identifiers.org/hco/13/GRCh38#19048760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48974155-C-A

19048760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974155-C-G

19048760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974155-C-T

19049141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974448-G-T

19049175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974483-C-T

19049590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974826-C-T

19049631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974882-T-A

19049631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48974882-T-G

http://identifiers.org/hco/13/GRCh38#19049952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48975000-C-A

19049952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 48975000-C-T

19050138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975537-T-C

19050148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975547-A-G

19050148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975547-A-T

19050396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975776-T-C

19050405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975782-G-A

19050507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975875-G-C

19050549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975915-C-T

19050570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975935-C-T

19050574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975939-G-A

http://identifiers.org/hco/13/GRCh38#19050618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48975971-C-A

19050618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48975971-C-G

19050670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976025-A-T

19050930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976230-C-G

19051026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976306-T-C

19051038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976318-T-C

19051111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976396-A-G

http://identifiers.org/hco/13/GRCh38#19051136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976402-A-C

19051136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976402-A-G

19051136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976402-A-T

19051281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48976545-T-C

19051299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48976566-G-A

19051299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48976566-G-C

19051299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48976566-G-T

http://identifiers.org/hco/13/GRCh38#19051302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976569-C-A

19051302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48976569-C-G

19051302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48976569-C-T

19051370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976645-A-G

19051371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976646-G-A

19051371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976646-G-T

19051445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976713-C-T

19051457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976731-G-A

19051457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976731-G-C

19051457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976731-G-T

19051464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976737-G-A

19051464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976737-G-T

http://identifiers.org/hco/13/GRCh38#19051475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48976748-C-A

19051475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976748-C-G

19051475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976748-C-T

19051613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976858-G-A

19051617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976862-G-C

19051722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48976927-G-A

19051785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48977000-G-A

19051948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978465-G-A

19051961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978479-G-A

19051973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978494-G-A

19052209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978748-A-G

19052309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978847-T-C

19052325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978881-G-T

19052339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978895-G-A

19052363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978919-A-G

19052383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978949-T-C

19052393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48978959-C-T

http://identifiers.org/hco/13/GRCh38#19052462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48979031-C-A

19052462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979031-C-T

19052660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979199-T-C

19052901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979482-T-C

19052901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979482-T-G

19052932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48979548-G-T

http://identifiers.org/hco/13/GRCh38#19053049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48979665-C-A

19053049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979665-C-T

19053087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979699-G-A

19053087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979699-G-T

19053094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979706-T-C

http://identifiers.org/hco/13/GRCh38#19053133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48979743-C-A

19053327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48979875-G-A

http://identifiers.org/hco/13/GRCh38#19053394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48979938-C-A

19056460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48982314-G-A

19056460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48982314-G-T

19056559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48982413-G-A

19056559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48982413-G-T

http://identifiers.org/hco/13/GRCh38#19056582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48982437-C-A

19056582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48982437-C-T

19059340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986200-G-A

19059387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986259-G-A

19059387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986259-G-C

19059431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986305-G-A

19060191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986640-C-T

http://identifiers.org/hco/13/GRCh38#19060276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48986701-A-C

19060479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986821-C-G

19060594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986955-C-T

19060637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48986997-G-A

19060642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987002-G-A

19060642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987002-G-T

19060914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987272-A-T

19060944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987301-G-A

19061000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987356-T-G

19061006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987362-G-A

19061008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987364-C-T

19061380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987580-G-A

19061409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987607-T-C

19061409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987607-T-G

19061415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987613-G-A

19061478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987680-G-A

19061478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987680-G-T

19061563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987862-A-G

http://identifiers.org/hco/13/GRCh38#19061575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48987874-A-C

19061614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48987909-G-T

19061833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988134-A-G

19061880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988166-T-C

19062013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988292-G-C

19062050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988321-G-A

19062056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988327-C-G

19062207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988430-G-A

19062207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988430-G-C

19062207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988430-G-T

http://identifiers.org/hco/13/GRCh38#19062295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48988492-C-A

http://identifiers.org/hco/13/GRCh38#19062306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48988503-A-C

http://identifiers.org/hco/13/GRCh38#19062452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48988630-C-A

19062452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988630-C-T

http://identifiers.org/hco/13/GRCh38#19062516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48988655-C-A

19062516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988655-C-T

19062576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988668-T-C

19062576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 48988668-T-G

19062643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48988735-G-A

19062643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48988735-G-T

19062693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48988784-G-A

19062693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48988784-G-T

http://identifiers.org/hco/13/GRCh38#19062713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#48988807-C-A

19062713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48988807-C-G

19062713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38808
most severe consequence: non coding transcript exon variant
orthologous variants: 48988807-C-T