72151271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021606-G-A

72151278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021609-G-T

72151316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021647-C-T

72151375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021708-T-C

72151398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021731-A-G

72151410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100021773-G-T

72151539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100021922-A-G

72151679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100021999-C-T

72151872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022172-C-T

72152062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022325-C-T

72152227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022473-C-T

72152393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022609-G-A

72152620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100022784-T-C

http://identifiers.org/hco/3/GRCh38#72152635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100022799-C-A

72152635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022799-C-T

72152660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022823-G-A

72152660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022823-G-T

72152731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100022856-A-G

72152918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 100023005-G-A

72152918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 100023005-G-C

72152918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 100023005-G-T

72152927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023018-C-G

72152927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023018-C-T

72152930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023021-T-C

http://identifiers.org/hco/3/GRCh38#72152939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023030-C-A

72152945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023036-G-A

72152945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023036-G-C

72152945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023036-G-T

72152956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100023046-C-T

http://identifiers.org/hco/3/GRCh38#72152974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023064-C-A

72152982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023072-G-A

72153024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023111-T-G

72153068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023153-A-G

http://identifiers.org/hco/3/GRCh38#72153075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023160-C-A

http://identifiers.org/hco/3/GRCh38#72153083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100023168-C-A

72153083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100023168-C-T

72153152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023234-C-G

72153269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023356-G-A

72153314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023400-A-G

72153702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100023748-C-T

http://identifiers.org/hco/3/GRCh38#72154153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100024126-C-A

72154222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100024191-T-C

72158834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028124-C-T

72158843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028133-G-A

72159073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028365-C-T

72159173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028461-G-A

72159173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028461-G-C

72159187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028475-C-T

72159200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028485-G-A

72159230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028520-G-T

72159232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028522-G-T

http://identifiers.org/hco/3/GRCh38#72159290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028575-C-A

72159313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028598-G-A

http://identifiers.org/hco/3/GRCh38#72159333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028614-C-A

http://identifiers.org/hco/3/GRCh38#72159400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028671-C-A

72159456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100028722-G-T

72159543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028766-G-A

72159543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028766-G-C

72159543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028766-G-T

72159579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028773-C-T

http://identifiers.org/hco/3/GRCh38#72159596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028783-C-A

72159628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100028809-A-G

http://identifiers.org/hco/3/GRCh38#72159667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100028853-C-A

72160236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030821-T-G

72160304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030880-T-G

72160338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100030908-C-T

72160494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031059-G-A

72160505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031070-C-T

72160527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031091-A-G

72160529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031093-T-C

72160529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031093-T-G

72160573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031136-A-T

72160933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100031461-G-A

http://identifiers.org/hco/3/GRCh38#72167305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100032636-A-C

72167305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032636-A-T

72167488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032807-G-T

72167783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100032965-G-A

72168032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033119-C-T

http://identifiers.org/hco/3/GRCh38#72168033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100033120-A-C

72168051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033122-C-T

72168059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033130-T-G

http://identifiers.org/hco/3/GRCh38#72168135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100033202-C-A

http://identifiers.org/hco/3/GRCh38#72168779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100033301-C-A

72169100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033619-C-T

72169412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100033908-T-C

72169570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034029-G-T

72169727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034466-G-A

72169889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034589-T-C

72169898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100034598-A-G

72170103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034747-G-A

72170345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034958-G-T

http://identifiers.org/hco/3/GRCh38#72170374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100034974-C-A

72170383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100034978-A-G

http://identifiers.org/hco/3/GRCh38#72170502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100035669-A-C

72170547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035716-G-T

72170567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035736-G-C

72170894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035782-G-A

72171011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100035899-A-T

72171340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036228-T-C

72171401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036280-G-A

72171401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036280-G-C

72171609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036489-G-C

72171649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036528-C-T

72171777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036640-T-A

72171777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036640-T-C

http://identifiers.org/hco/3/GRCh38#72171784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100036647-A-C

72171784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036647-A-G

http://identifiers.org/hco/3/GRCh38#72171794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100036657-A-C

72171794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100036657-A-G

http://identifiers.org/hco/3/GRCh38#72171906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100036768-C-A

72171991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100036848-G-A

72172403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100037250-G-A

72172403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100037250-G-T

72172545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100037377-A-G

72173071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040115-T-G

72173092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040136-T-C

72173152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040196-G-T

72173235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040268-T-C

72173254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040287-C-T

http://identifiers.org/hco/3/GRCh38#72173311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100040320-C-A

72173320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040329-T-C

72173446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040434-A-G

72173455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040443-T-G

http://identifiers.org/hco/3/GRCh38#72173498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100040472-C-A

72173498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040472-C-T

72173501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040475-T-C

http://identifiers.org/hco/3/GRCh38#72173525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100040532-C-A

72173525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040532-C-G

72173531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040538-C-T

72173661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040703-G-A

72173661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100040703-G-T

72174201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100041464-T-C

72174300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100041578-G-T

72174453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041686-A-G

72174508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041722-C-T

http://identifiers.org/hco/3/GRCh38#72174516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100041730-A-C

72174516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100041730-A-G

http://identifiers.org/hco/3/GRCh38#72174820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100041985-C-A

72175026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042147-C-T

72175149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042257-A-G

72175280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042523-T-C

72175345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042584-C-T

72175361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042605-C-T

72175389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100042635-A-G

72175669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043837-C-T

72175768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043923-C-G

72175804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043959-G-A

72175814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043982-C-T

72175819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043987-T-C

72175819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100043987-T-G

http://identifiers.org/hco/3/GRCh38#72175846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100044014-C-A

72176879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044151-C-T

72177216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044393-G-A

72177263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044442-G-A

72177303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044474-C-T

72177598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100044754-T-C

72177607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100044763-G-T

72178380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046359-G-A

72178380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046359-G-T

72178388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046367-G-A

72178388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046367-G-C

72178388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046367-G-T

72178396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046375-G-A

72178396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046375-G-T

72178478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046458-A-G

72178478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046458-A-T

72178537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046504-G-T

http://identifiers.org/hco/3/GRCh38#72178602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100046578-C-A

72178611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046587-C-T

72178617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100046593-G-A

http://identifiers.org/hco/3/GRCh38#72178656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100046639-C-A

72178814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046778-T-A

72178814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100046778-T-C

72179135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100047184-G-A

72179939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100048070-G-T

72182778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051526-G-A

72183030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051733-C-T

72183068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100051767-G-A

72183355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052034-T-C

72184505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100052374-T-C

72185997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100056073-C-T

72185998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100056074-T-C

72186259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100056348-T-C

72189815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100057819-C-T

72189820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100057824-G-A

72189855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100057860-G-C

72191073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059091-T-C

72191176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059178-T-C

72191193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059195-G-A

72191339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059342-G-C

72191430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059432-G-C

72191439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059441-C-T

72191469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059471-C-T

72191482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059484-G-A

72191507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059508-T-C

72191509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059510-G-A

http://identifiers.org/hco/3/GRCh38#72191521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100059515-C-A

http://identifiers.org/hco/3/GRCh38#72191572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100059563-A-C

72191572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059563-A-G

72191572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059563-A-T

72191575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059566-T-A

72191575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059566-T-C

72191836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059788-A-G

72192022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100059981-A-G

72192075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060033-A-G

72192089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060047-C-T

72192693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060609-C-G

72192693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060609-C-T

72192794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100060685-C-T

72193171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100061865-T-C

72193659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100062488-C-T

72193930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100062781-C-G

72194391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063190-C-T

72194424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063223-C-T

72195686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063727-T-C

72195751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063795-T-G

72195882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063893-C-T

72195894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063905-C-T

72195896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100063907-A-G

72196176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064128-C-T

72196224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064151-G-A

72196224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064151-G-T

72196271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064192-T-C

72196307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064227-T-C

72196564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064484-G-A

72196590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064510-C-G

72196612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064531-G-C

72196612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100064531-G-T

72197613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100065924-T-A

72197728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066034-A-T

72197781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066078-G-C

72197816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066112-G-A

72198010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066242-C-T

72198400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066741-T-C

http://identifiers.org/hco/3/GRCh38#72198493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100066830-C-A

72198495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100066832-A-G

72202647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068187-G-T

72202772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068301-G-A

72203010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068521-G-T

72203258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068749-T-C

72203377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100068912-T-A

72203444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100068991-G-T

72203479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069029-A-G

72203517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069067-A-G

72203523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069073-G-T

72203629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069172-G-A

72203767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069288-T-A

72203780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069303-C-T

72203917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069411-A-G

72203966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069460-G-A

72203966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069460-G-T

72204018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069512-G-A

72204043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069539-G-A

72204043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069539-G-T

http://identifiers.org/hco/3/GRCh38#72204063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100069560-A-C

72204063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069560-A-G

72204102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069593-T-C

72204162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100069657-G-A

72204268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069752-T-C

72204318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069803-G-A

72204318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100069803-G-T

http://identifiers.org/hco/3/GRCh38#72204789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100070217-A-C

72204885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070260-T-A

72204885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070260-T-C

72204892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070264-A-G

72204976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070355-G-A

72205034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100070409-G-A

72205589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072773-T-A

72205602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072786-G-A

72205625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072809-G-A

72205625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072809-G-T

72205638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072821-C-G

72205651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100072834-G-A

72205930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100073053-C-T

72206247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100073375-G-C

72206255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100073383-G-T

72206518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100073649-A-G

72207255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100074989-G-A

72207363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075086-G-A

72207503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075207-G-T

72207649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075359-C-T

72207767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100075476-G-A