100261201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051546-T-A

100261201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051546-T-C

http://identifiers.org/hco/3/GRCh38#100261234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57051518-C-A

100261234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57051518-C-T

100261348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57051428-T-C

100261463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051324-G-C

100261463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051324-G-T

100261471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051316-G-A

100261471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051316-G-C

100261471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57051316-G-T

http://identifiers.org/hco/3/GRCh38#100261508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57051283-C-A

100261562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57051214-T-C

100261595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57051181-T-G

100261608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57051168-C-T

http://identifiers.org/hco/3/GRCh38#100261610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57051166-C-A

100262063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050555-A-G

100262260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57050460-G-A

100263853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57049505-A-G

100264053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57048764-C-T

100264101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57048724-T-G

100264111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57048715-G-A

100264111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57048715-G-T

http://identifiers.org/hco/3/GRCh38#100264147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57048675-A-C

100264736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047845-C-T

100264946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047432-G-A

100264965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57047416-G-A

100265671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57046494-A-G

100265671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57046494-A-T

100266850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57046277-C-T

100269785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57043236-T-C

100275647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042911-A-G

100275841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042767-A-G

100275843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042765-A-G

100275919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042684-A-G

100276020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042599-G-A

100276036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57042583-A-T

100276551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041884-C-T

100276553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041882-T-G

http://identifiers.org/hco/3/GRCh38#100276589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57041846-C-A

100276682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041785-T-A

100276682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041785-T-C

100276823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041496-A-G

100277062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041291-C-T

http://identifiers.org/hco/3/GRCh38#100277081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57041275-C-A

100277081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041275-C-T

100277124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57041254-T-A

http://identifiers.org/hco/3/GRCh38#100277445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57040975-C-A

100277456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040964-G-A

100277800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040634-T-G

http://identifiers.org/hco/3/GRCh38#100277855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57040577-C-A

100278011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040447-G-A

http://identifiers.org/hco/3/GRCh38#100278109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57040354-A-C

100278218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57040264-G-T

100278763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039863-A-G

100279256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039314-C-T

100279270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57039256-T-C

100279465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57038997-T-A

100279501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57038977-A-G

100279608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57038884-T-G

http://identifiers.org/hco/3/GRCh38#100279772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57038658-C-A

100279772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038658-C-T

http://identifiers.org/hco/3/GRCh38#100279795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57038635-C-A

http://identifiers.org/hco/3/GRCh38#100279872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57038577-C-A

100279872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038577-C-T

100280027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038531-A-G

100280108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57038460-G-A

100280488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57037328-A-G

100281419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034920-A-G

100281461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034875-A-T

100281618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034735-T-C

100281618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034735-T-G

100281635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034718-T-C

100281635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57034718-T-G

http://identifiers.org/hco/3/GRCh38#100281719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#57034647-C-A

http://identifiers.org/hco/3/GRCh38#100281746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57034626-C-A

100281746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57034626-C-T

100281849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 57034523-T-C

http://identifiers.org/hco/3/GRCh38#100281964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57034455-C-A

100282869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033531-C-T

100283353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033167-G-A

100283473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033059-T-C

100283473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033059-T-G

100283485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033047-G-T

100283509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57033024-G-C

100283836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57032713-G-C

100283841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57032708-T-A

100287381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031406-T-G

100287398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031389-G-A

100287415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031372-G-A

100287473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031315-G-C

100287540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031260-C-T

100287544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031256-T-A

100287599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031205-C-T

100287689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031145-G-A

100287710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031120-A-G

100287793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031055-T-C

100287805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031043-A-T

100287868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031003-C-G

100287868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57031003-C-T

100288214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030550-C-T

100288328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030457-T-A

100288574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57030221-A-G

100289425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029704-C-T

100289469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029668-C-T

100289481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029658-A-G

100289562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029583-A-T

100289592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029525-G-A

100289736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029398-T-C

100289961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029289-G-A

100290150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029118-A-G

100290203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029070-G-T

100290254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57029021-G-T

100290490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028796-T-C

100290491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028795-G-A

100290492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028794-T-G

100290514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028748-G-A

100290514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028748-G-C

100290514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028748-G-T

100290663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57028603-A-G

http://identifiers.org/hco/3/GRCh38#100290827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57028468-A-C

100290827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028468-A-G

100291141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57028189-T-C

100292130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021335-G-A

100292398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021075-T-A

http://identifiers.org/hco/3/GRCh38#100292399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57021074-C-A

100292458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57021026-C-T

100293670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57020428-T-C

100293741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57020366-C-T

100293839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57020290-C-T

100294089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57020168-A-T

100294831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019565-C-T

100294941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 57019454-G-A

100294941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57019454-G-T

http://identifiers.org/hco/3/GRCh38#100294989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57019430-A-C

http://identifiers.org/hco/3/GRCh38#100295012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57019407-C-A

100295053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019372-G-A

http://identifiers.org/hco/3/GRCh38#100295062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57019363-C-A

100295062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019363-C-G

100295132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57019299-G-A

100295221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019210-T-C

100295224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019207-T-C

100295274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019159-C-G

100295274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019159-C-T

100295280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019153-T-C

100295376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57019065-A-G

100296155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57018765-T-C

http://identifiers.org/hco/3/GRCh38#100296190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57018727-C-A

http://identifiers.org/hco/3/GRCh38#100296341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57018570-A-C

100296341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57018570-A-G

100296341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57018570-A-T

http://identifiers.org/hco/3/GRCh38#100296375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57018532-C-A

100296375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57018532-C-T

100296385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57018522-A-T

100297842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013170-T-A

100297842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013170-T-G

100297865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57013149-T-C

100297965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57013050-G-A

100298068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012948-G-A

100298068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012948-G-C

http://identifiers.org/hco/3/GRCh38#100298103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57012813-A-C

100298103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012813-A-G

http://identifiers.org/hco/3/GRCh38#100298197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57012731-A-C

100298225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012706-G-A

http://identifiers.org/hco/3/GRCh38#100298297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57012643-C-A

100298339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012601-A-G

100298893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012242-A-G

100298949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012205-A-T

100299098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012090-G-T

100299108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012074-T-A

100299142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57012041-G-T

100299183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011983-G-T

http://identifiers.org/hco/3/GRCh38#100299188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57011978-A-C

100299188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011978-A-G

100299188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011978-A-T

100299339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57011827-T-A

http://identifiers.org/hco/3/GRCh38#100299405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57011756-C-A

100299405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011756-C-T

100299421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011742-T-G

100299867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011652-C-G

100299903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011618-C-T

100300213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011303-T-C

http://identifiers.org/hco/3/GRCh38#100300397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57011076-A-C

100300431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57011042-C-T

100300839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57010956-G-A

100301018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57010794-T-A

100301585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57010223-G-T

http://identifiers.org/hco/3/GRCh38#100301729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57010084-C-A

100301822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009985-A-G

100302051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57009808-T-A

100302100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57009760-G-A

100302112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57009748-C-G

100302131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57009729-C-G

100302154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57009706-G-A

100302248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009612-A-G

100302272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57009589-T-A

100302982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008045-A-G

http://identifiers.org/hco/3/GRCh38#100302984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57008043-A-C

100302986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008041-A-G

100302988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57008039-A-G

100304489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007384-T-G

100304576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007300-G-A

100304636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007244-C-T

100304737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007148-G-A

100304737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007148-G-T

100304812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57007075-T-C

100304946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57006938-T-A

100306171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005084-C-T

100306192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005064-A-G

100306230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57005044-A-G

http://identifiers.org/hco/3/GRCh38#100306340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57004944-C-A

100306340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004944-C-T

http://identifiers.org/hco/3/GRCh38#100306351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57004933-C-A

100306351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004933-C-T

100306360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004924-T-A

100306360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004924-T-C

http://identifiers.org/hco/3/GRCh38#100306385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57004899-C-A

100306385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004899-C-T

100306487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57004797-T-G

100306588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004669-C-T

100306600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004657-T-C

100306606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004651-A-G

100306608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004649-T-A

100306608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004649-T-C

100306608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004649-T-G

http://identifiers.org/hco/3/GRCh38#100306652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57004608-C-A

http://identifiers.org/hco/3/GRCh38#100306653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57004607-A-C

100306684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004578-A-G

100307310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57004318-A-G

http://identifiers.org/hco/3/GRCh38#100310318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57003434-C-A

100310318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003434-C-G

100310318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003434-C-T

http://identifiers.org/hco/3/GRCh38#100310322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57003430-C-A

100310322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003430-C-G

100310322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003430-C-T

http://identifiers.org/hco/3/GRCh38#100310445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57003309-C-A

100310558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57003198-A-G

100311003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002804-A-G

100311037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002772-A-G

100311187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002516-A-G

100311269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002436-C-T

100311380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002351-G-A

100311478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002254-T-C

100311619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002115-T-C

100311654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002078-C-T

100311660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002066-T-C

100311698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002028-G-A

100311698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57002028-G-T

100311890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001840-G-A

http://identifiers.org/hco/3/GRCh38#100311896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57001834-C-A

http://identifiers.org/hco/3/GRCh38#100311910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57001820-C-A

100311929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001803-G-A

http://identifiers.org/hco/3/GRCh38#100311941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57001791-C-A

100311941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001791-C-G

100312000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001729-T-C

100312000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001729-T-G

http://identifiers.org/hco/3/GRCh38#100312004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57001725-C-A

100312004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001725-C-T

100312235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001504-A-G

100312301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001409-T-G

100312336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57001337-T-G

100313412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57000371-C-T

100314009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56999435-A-T

http://identifiers.org/hco/3/GRCh38#100314071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56999356-C-A

http://identifiers.org/hco/3/GRCh38#100314840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56999116-A-C

100315556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998907-G-C

100315818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998662-T-C

100315818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998662-T-G

100315821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998659-G-A

100316028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56998451-A-T

http://identifiers.org/hco/3/GRCh38#100316200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56998277-A-C

100316200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998277-A-G

100316203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998274-T-G

http://identifiers.org/hco/3/GRCh38#100316225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56998253-C-A

100316225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56998253-C-T

100319111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56993478-A-G

http://identifiers.org/hco/3/GRCh38#100319143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56993446-C-A

http://identifiers.org/hco/3/GRCh38#100319272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56993323-C-A

100319272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56993323-C-T

http://identifiers.org/hco/3/GRCh38#100319930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56993032-C-A

100320010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992995-T-C

100320028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992982-T-C

100320102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992935-C-T

100320256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992826-T-C

100320309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992761-T-C

100320633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992297-A-G

100320729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56992207-A-G

100321063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991901-G-A

100321099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991856-A-G

100321109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991846-A-G

100321109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991846-A-T

http://identifiers.org/hco/3/GRCh38#100321111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56991844-C-A

100321121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991834-G-A

http://identifiers.org/hco/3/GRCh38#100321155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56991808-A-C

100323180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56991097-G-A

100323370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56990922-C-G

100323439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56990887-A-T

100324100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56990300-T-G

100324139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56990260-A-G

100324229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56990175-C-T

100324242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56990164-G-T

100324612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56989810-C-T

100324619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56989803-T-C

100324630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56989792-T-C

100324636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56989786-T-C

100324639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56989783-A-G

100324842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56989613-A-G

http://identifiers.org/hco/3/GRCh38#100325097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56989354-C-A

http://identifiers.org/hco/3/GRCh38#100325145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#56989320-C-A

100325243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25622
most severe consequence: 3 prime UTR variant
orthologous variants: 56989217-G-T