112055905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435055-G-A

http://identifiers.org/hco/13/GRCh38#112056373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12435444-C-A

112056373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435444-C-T

112056519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12435557-C-T

112056854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12435873-G-A

112056900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12435924-G-A

112057139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12436139-G-A

112057203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436201-A-G

112057203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436201-A-T

112057733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436722-C-T

112057785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436770-G-A

112057967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12436964-C-T

112058039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437036-G-A

112058287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437295-G-A

112058736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437633-G-A

112058957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437900-C-T

112059050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437981-G-C

112059050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12437981-G-T

112059469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438428-T-A

112059504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438463-C-T

112059513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438472-G-A

112059513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438472-G-T

112059636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12438577-C-G

112060435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439366-A-G

http://identifiers.org/hco/13/GRCh38#112060694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12439639-C-A

112060832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439775-T-C

112060846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439789-G-A

112060866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439813-G-A

112060896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12439843-A-G

112061087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440012-C-G

112061087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440012-C-T

112061375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440269-C-T

112061497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440369-C-T

112061530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440397-G-A

112061530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440397-G-C

112061543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440405-C-T

112061651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12440533-C-G

http://identifiers.org/hco/13/GRCh38#112062403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12441206-C-A

http://identifiers.org/hco/13/GRCh38#112062420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12441223-A-C

112062423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441226-G-A

112062840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12441639-C-T

112062890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441689-G-A

112062890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12441689-G-C

http://identifiers.org/hco/13/GRCh38#112063205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12441941-C-A

112063608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12442276-C-T

112064005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12442726-A-G

112064291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12442995-G-A

http://identifiers.org/hco/13/GRCh38#112064312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12443012-C-A

http://identifiers.org/hco/13/GRCh38#112065092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12443756-A-C

112065122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12443786-G-T

112065486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444107-C-G

112065513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444138-G-A

112065623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444271-G-A

112065808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444473-C-T

http://identifiers.org/hco/13/GRCh38#112065921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12444624-A-C

112065972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444675-G-A

112066293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12444974-G-A

112066518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445208-G-A

112066527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445217-T-A

112066527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445217-T-C

112066717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445419-G-A

112066754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445458-T-G

112066928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445636-G-A

112066961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445669-C-G

112067050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445757-G-A

112067050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445757-G-C

112067071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12445778-G-A

112067306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12445997-G-C

112067401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446080-C-T

http://identifiers.org/hco/13/GRCh38#112067550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12446236-C-A

112067550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446236-C-T

http://identifiers.org/hco/13/GRCh38#112067667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12446369-C-A

112067667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446369-C-G

112067667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446369-C-T

112067793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446495-G-A

112067793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446495-G-C

112067793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446495-G-T

112067949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446651-G-A

112068000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446702-G-A

112068000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446702-G-C

112068000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446702-G-T

http://identifiers.org/hco/13/GRCh38#112068072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12446774-C-A

112068072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446774-C-T

http://identifiers.org/hco/13/GRCh38#112068153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12446855-C-A

112068153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446855-C-G

112068153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12446855-C-T

http://identifiers.org/hco/13/GRCh38#112068408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447110-C-A

112068408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447110-C-G

112068408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447110-C-T

112068549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447251-G-A

112068549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447251-G-C

112068570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447272-G-A

112068570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447272-G-C

112068570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447272-G-T

http://identifiers.org/hco/13/GRCh38#112068603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447305-C-A

112068603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447305-C-G

112068603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447305-C-T

http://identifiers.org/hco/13/GRCh38#112068669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447371-C-A

112068669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447371-C-G

112068669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447371-C-T

112068717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447419-G-A

112068717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447419-G-T

http://identifiers.org/hco/13/GRCh38#112068744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447446-C-A

112068744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447446-C-G

112068744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447446-C-T

112068843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447545-G-A

112068843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447545-G-C

112068843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447545-G-T

http://identifiers.org/hco/13/GRCh38#112068890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447605-C-A

112068890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447605-C-G

112068890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447605-C-T

http://identifiers.org/hco/13/GRCh38#112068940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447642-C-A

112068940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447642-C-G

112068986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447689-G-A

112068986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447689-G-C

112068986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447689-G-T

112069077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447768-T-A

112069077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447768-T-C

http://identifiers.org/hco/13/GRCh38#112069136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447827-C-A

112069136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447827-C-T

112069250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447938-A-G

http://identifiers.org/hco/13/GRCh38#112069277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12447969-A-C

112069277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12447969-A-G

112069546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448221-G-C

http://identifiers.org/hco/13/GRCh38#112069744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12448427-C-A

112069744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448427-C-T

112069778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448457-A-G

112069872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448558-T-C

112069875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448561-G-A

112069875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448561-G-C

112069905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448596-T-C

http://identifiers.org/hco/13/GRCh38#112069940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12448630-C-A

112069940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448630-C-T

112070051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448727-G-A

http://identifiers.org/hco/13/GRCh38#112070104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12448779-A-C

http://identifiers.org/hco/13/GRCh38#112070260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12448935-C-A

112070260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448935-C-T

112070262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12448937-T-C

112070341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12449016-G-C

112070411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12449089-T-C

112070416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12449094-T-G

112071366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12450028-C-T

112071651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12450284-A-G

112071667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12450300-T-C

http://identifiers.org/hco/13/GRCh38#112072039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12450696-C-A

112072231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450894-T-C

112072325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450991-G-A

112072610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451199-G-A

112072778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451340-C-T

http://identifiers.org/hco/13/GRCh38#112072798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12451359-C-A

112072798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451359-C-T

112072978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451541-C-T

112073012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451575-G-A

112073013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451576-T-A

112073016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451579-C-T

http://identifiers.org/hco/13/GRCh38#112073375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12451834-C-A

112073476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451914-C-T

112073481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451919-G-A

112073753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452155-G-A

112074344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452710-G-A

112074544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452913-G-C

112074590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452957-C-G

112074624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452989-G-A

112074631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452996-G-T

112075150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453489-G-C

112075337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453658-G-C

112075466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453737-G-A

112075510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453785-G-A

112076031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454187-T-C

112076033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454189-T-C

112076367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454420-C-T

112076404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454461-G-C

112076417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454475-G-A

112076574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454667-G-T

112076691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454775-G-C

112076760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454885-T-A

112076827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454945-A-G

112076966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455036-T-C

112077254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455174-A-G

112077286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455207-A-G

112077408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455324-T-G

http://identifiers.org/hco/13/GRCh38#112077435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12455369-C-A

112077578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455503-G-C

112077638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455559-A-G

112077719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455642-C-T

112077795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455707-T-G

112077873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455777-C-T

http://identifiers.org/hco/13/GRCh38#112077924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12455815-C-A

112077924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455815-C-G

112077924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455815-C-T

http://identifiers.org/hco/13/GRCh38#112077991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12455869-A-C

112079920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12456990-A-T

112080041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12457125-G-A

112080133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457298-T-G

112080147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457310-G-A

112080575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457718-T-G

112080786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12457941-C-G

112080896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458049-A-G

112080927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458080-A-G

112080927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458080-A-T

112080952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458113-A-G

112081151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458317-C-G

112081167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458333-A-G

112081993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12458781-G-A

112082835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460107-G-A

http://identifiers.org/hco/13/GRCh38#112082896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12460162-C-A

112083387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460715-A-G

112083423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12460751-G-T

http://identifiers.org/hco/13/GRCh38#112083467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12460787-C-A

112083679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461001-A-T

112083738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461053-C-T

112083809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461101-A-G

http://identifiers.org/hco/13/GRCh38#112084042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12461450-C-A

112084042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461450-C-T

112084062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461477-A-G

112084237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461679-T-C

112084394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461828-T-C

112084500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461933-A-G

112084598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12462054-T-A

112086527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465211-G-A

112086543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465227-A-G

112086559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465248-C-T

112086591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465280-C-T

112086691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465360-G-A

112086691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465360-G-C

112086691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465360-G-T

112087474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466085-G-A

112087613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466235-C-G

112087861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466487-T-C

112087863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466489-C-T

112087895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466524-G-A

112087908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466538-G-A

112088322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466933-T-C

112088327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466938-G-A

112088327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466938-G-T

112089127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467298-T-C

112089206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467366-T-C

112089406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467552-T-A

112089465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467610-T-C

112089465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467610-T-G

112089544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467778-A-G

112089558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467792-G-A

112089926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468133-C-T

112090050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468255-G-C

112090146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468334-T-C

112090184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468349-C-T

112097329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12473941-G-A

112097338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12473951-C-T

http://identifiers.org/hco/13/GRCh38#112097572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12474167-A-C

112097645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474238-C-T

112098020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474597-G-C

112098024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474600-G-A

112098133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474710-C-T

112098379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: non coding transcript exon variant
orthologous variants: 12474937-G-C

112098785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12475206-G-T

112098847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12475257-G-A

112098858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12475268-C-T

112099716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12476582-C-T

112099717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12476583-G-A

112099736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12476602-C-G

112099736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12476602-C-T

http://identifiers.org/hco/13/GRCh38#112099869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12476735-C-A

112099886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12476752-T-G

http://identifiers.org/hco/13/GRCh38#112100379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12477137-C-A

112100427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12477167-G-C

112100427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12477167-G-T

112100704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12477414-G-A

112100704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12477414-G-T

112101100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12477530-C-G

112102161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12478552-G-A

112102161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12478552-G-T

112102428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12478818-G-T

112102819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479197-T-C

112102864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479242-A-G

112102873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479251-C-G

112102873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479251-C-T

112103029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479379-G-T

112103079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479427-G-A

112103079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479427-G-T

112103210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479546-C-T

112103390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479695-A-G

112103682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12479908-C-T

112103727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12479953-C-G

112103840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12480054-G-A

112104606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12480775-C-G

112104714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12480880-C-T

112104718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12480884-G-A

112104917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12481050-G-A

112104917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12481050-G-C

112105134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12481249-C-T

112105156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12481273-C-G

112105400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12481512-C-T

112105637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12481699-G-A

http://identifiers.org/hco/13/GRCh38#112105743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#12481793-A-C

112105744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12481794-G-A

112105841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12481871-C-T

112106233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12482320-G-T

http://identifiers.org/hco/13/GRCh38#112106371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12482449-C-A

112106404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12482481-T-C

112106467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12482537-A-G

112106564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12482608-T-C

http://identifiers.org/hco/13/GRCh38#112106700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12482726-C-A

112106700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12482726-C-T

112106868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12482888-G-A

112106882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12482902-T-A

112106946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12482964-G-A

112106946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12482964-G-T

112107044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12483030-G-C

112107044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12483030-G-T

http://identifiers.org/hco/13/GRCh38#112107153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42733
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#12483130-C-A