http://identifiers.org/hco/4/GRCh38#99950054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137570572-C-A

http://identifiers.org/hco/4/GRCh38#99950084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137570542-C-A

99950084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570542-C-G

99950084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570542-C-T

http://identifiers.org/hco/4/GRCh38#99950089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137570533-C-A

99950089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570533-C-T

99950151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570472-G-A

99950151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570472-G-C

99950151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570472-G-T

http://identifiers.org/hco/4/GRCh38#99950237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137570386-C-A

99950237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137570386-C-G

99950237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137570386-C-T

99950386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570237-G-T

99950412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570211-G-T

99950430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570193-G-A

99950430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570193-G-C

99950431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570192-G-C

99950431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570192-G-T

http://identifiers.org/hco/4/GRCh38#99950432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137570191-C-A

99950432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570191-C-G

99950432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570191-C-T

99950476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570147-G-A

99950476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137570147-G-T

99950529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570087-G-A

99950529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137570087-G-T

http://identifiers.org/hco/4/GRCh38#99950589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137570036-C-A

99950639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569965-G-C

99950639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569965-G-T

99950685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569919-G-A

99950695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569912-G-A

99950695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569912-G-C

99950695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569912-G-T

99950774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569849-A-G

99950823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569815-G-A

99950823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569815-G-C

99950823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137569815-G-T

99952485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137567397-T-G

99952530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137567352-C-G

99952530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137567352-C-T

99953454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137563876-A-G

99955241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137562226-C-G

http://identifiers.org/hco/4/GRCh38#99955319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137562117-C-A

99961199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137558197-T-C

99962188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137555015-T-A

99962188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137555015-T-C

99962769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137554573-C-T

http://identifiers.org/hco/4/GRCh38#99965904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137551379-C-A

99986258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137537118-C-T

http://identifiers.org/hco/4/GRCh38#99986399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137536916-C-A

99986419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137536896-G-A

99986562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137536757-A-G

99986689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137536651-G-A

99986815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137536519-G-A

99987545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137533838-T-C

99987778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137533600-C-G

99989158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137528476-A-G

http://identifiers.org/hco/4/GRCh38#99989191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137528454-A-C

99991670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137528125-G-A

99991684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137528111-A-G

99991811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137527966-G-T

http://identifiers.org/hco/4/GRCh38#99991837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137527944-C-A

99991948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137527841-G-A

99992932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137527020-T-A

http://identifiers.org/hco/4/GRCh38#99993018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137526939-C-A

99993018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137526939-C-G

http://identifiers.org/hco/4/GRCh38#99996630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137526096-C-A

99996631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137526095-C-T

99996700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137526026-T-C

99996813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137525913-G-A

99997020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137525725-T-C

99997020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137525725-T-G

99997022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137525723-A-G

99997942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524891-T-C

99998097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524739-C-T

99998118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524716-T-C

99998297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524413-C-T

99998315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524384-G-A

99998432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524193-G-A

99998520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524106-T-C

99998528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524098-A-G

99998528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137524098-A-T

100000413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137522579-G-C

100000414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137522578-G-A

100006745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137522295-C-G

100007952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137518989-A-G

http://identifiers.org/hco/4/GRCh38#100008115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137518859-C-A

100008115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137518859-C-T

http://identifiers.org/hco/4/GRCh38#100008133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137518841-C-A

100008133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137518841-C-T

100009184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

100009238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

100025263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137512579-A-G

http://identifiers.org/hco/4/GRCh38#100025277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137512563-C-A

100025319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137512522-T-C

100025864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137511991-G-C

100025910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137511947-A-G

100026150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137511717-A-G

http://identifiers.org/hco/4/GRCh38#100026188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137511669-A-C

100026640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137508433-G-A

100026854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137508225-T-C

100033740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137508060-C-T

100033930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137507911-T-C

http://identifiers.org/hco/4/GRCh38#100033947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137507894-C-A

100033947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137507894-C-T

100034233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137507629-T-C

100034257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137507605-C-G

100034257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137507605-C-T

100034860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137506228-C-G

100034860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137506228-C-T

100034891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137506201-G-A

100035083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137505711-T-A

100035083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137505711-T-G

100037412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137505655-A-G

100037500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137505579-A-G

100037669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137505292-T-C

100037670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137505291-G-A

100037670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137505291-G-T

100037730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137505236-G-A

100037730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137505236-G-T

100037736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137504920-T-C

100037753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137504903-G-C

100037776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: non coding transcript exon variant
orthologous variants: 137504893-A-T

100037905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137504774-T-C

100037934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137504746-G-A

100037934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137504746-G-T

100037956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137504722-G-A

100037964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137504708-C-T

100038067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137504622-G-A

100039840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137503042-A-G

100039843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137503039-C-T

100040060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137502839-G-C

100040099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137502789-G-C

http://identifiers.org/hco/4/GRCh38#100042790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137502037-A-C

100042790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137502037-A-G

100042799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137502029-G-A

100042801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137502027-G-A

100042801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137502027-G-T

100049588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137501128-A-T

http://identifiers.org/hco/4/GRCh38#100049849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137500461-C-A

100049879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500432-C-T

100049893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500418-A-T

100050010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500295-T-C

100050174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500155-A-G

100050177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500152-T-A

100050177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500152-T-C

100050235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500089-T-G

100050283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500033-T-C

100050283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137500033-T-G

100050522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137499628-T-A

100055090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137497757-C-T

100055180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137497674-T-C

100055220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137497631-A-G

http://identifiers.org/hco/4/GRCh38#100055474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137497420-C-A

http://identifiers.org/hco/4/GRCh38#100056077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137496873-C-A

100056504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137496506-T-C

100057154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137495034-A-G

http://identifiers.org/hco/4/GRCh38#100057215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137494975-C-A

100057274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137494915-G-A

100057555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137494655-C-T

100057666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137494498-G-A

http://identifiers.org/hco/4/GRCh38#100057842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137493776-A-C

100057931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137493687-G-A

100058478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137493499-A-G

100058484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137493493-A-G

100058557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137493415-T-G

100059546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137489271-G-A

100059663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137489162-C-T

100060285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137486881-A-G

100060445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137486686-A-T

100060489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137486649-A-G

100060587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137486422-A-G

100060653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137486356-C-G

100061035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137485964-A-G

100061192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137485844-G-A

100061228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137485808-G-A

100063583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137484075-C-T

100063608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137484050-C-T

http://identifiers.org/hco/4/GRCh38#100063826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137483834-C-A

100063973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137483695-G-A

100064048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137483634-C-T

100064061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137483620-G-A

100064130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137483535-T-C

http://identifiers.org/hco/4/GRCh38#100064184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137483484-A-C

100065750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137482109-T-C

100066013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137481828-T-A

100066013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137481828-T-C

http://identifiers.org/hco/4/GRCh38#100066075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137481772-A-C

http://identifiers.org/hco/4/GRCh38#100066117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137481737-C-A

http://identifiers.org/hco/4/GRCh38#100067142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137480926-C-A

100067146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137480922-C-G

100067159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137480909-A-T

100070674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137474049-T-C

100070717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137474005-C-G

100070732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137473990-A-G

100070941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137473828-T-A

http://identifiers.org/hco/4/GRCh38#100070964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137473804-C-A

100071153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137473603-C-T

100071178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137473575-A-G

100071260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137473490-C-T

100077636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137469124-T-C

100077704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137469056-A-G

100077979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137468804-G-A

100078000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137468783-C-T

100078664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137468126-C-T

100078711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137468042-G-A

http://identifiers.org/hco/4/GRCh38#100078791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137467964-C-A

100078791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137467964-C-T

100082347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137465470-T-A

100082416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137465398-G-T

100082636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137464478-T-C

100082894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137464244-G-C

100083066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137464097-T-A

100083424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463761-G-A

100083461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463724-C-T

100083466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463719-C-T

100083649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463545-A-T

100083665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463529-T-C

100083726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463468-T-C

100083727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463467-G-T

100083768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463425-G-A

100083841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463341-A-G

100083850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463327-C-G

100083850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137463327-C-T

http://identifiers.org/hco/4/GRCh38#100083868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137463309-C-A

100085312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137462087-G-A

100085807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137461535-A-T

100088369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137461450-T-A

100088450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137461370-A-G

100088514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137461307-A-G

http://identifiers.org/hco/4/GRCh38#100093063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137459375-A-C

100093150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137459283-C-T

100093205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137459231-C-T

100093242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137459195-A-G

100093317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137459138-G-C

100093470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137458997-T-C

100093597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137458861-T-C

100093619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137458833-C-G

100094211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137458278-T-C

100094524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137457816-G-C

100094915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137457536-A-G

100095254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137457181-G-A

100095514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137455745-G-A

100095774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137455493-C-T

100095973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137455167-C-T

100096068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137455084-G-A

100096164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137454964-G-A

100096182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137454943-G-A

100096200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137454924-C-T

100096233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137454900-G-A

100096452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137454656-T-A

100096452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137454656-T-G

http://identifiers.org/hco/4/GRCh38#100096542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137454580-A-C

100096542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137454580-A-T

100096623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137454515-A-G

http://identifiers.org/hco/4/GRCh38#100096713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137454430-A-C

100100442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137452234-G-A

100100445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137452231-T-C

100100467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137452209-G-A

http://identifiers.org/hco/4/GRCh38#100100668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137451968-C-A

http://identifiers.org/hco/4/GRCh38#100101085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137451035-C-A

100101117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137451004-G-C

100101117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137451004-G-T

http://identifiers.org/hco/4/GRCh38#100101222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137450899-A-C

100101434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137450709-T-C

100101526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137450592-T-A

100101669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137450127-A-G

100101727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137450069-T-C

100101753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137450043-A-G

100101884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137449920-T-A

100102251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137449630-T-A

100102498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137449328-G-A

100102941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137448608-T-C

100102944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137448605-T-G

100103192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137448417-G-A

100103386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137448254-G-T

100103481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137448112-C-T

100103686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137447924-A-G

100105514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137439621-G-A

100105635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137439515-G-T

100105741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137439268-T-C

100105829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137439170-T-C

100106005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137439003-T-C

http://identifiers.org/hco/4/GRCh38#100106357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137438613-A-C

100106828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137438012-A-G

100106845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137437995-T-C

100106886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137437957-G-A

100108263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137434888-A-G

100108522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137434673-G-C

100108920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137434149-G-A

100108986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137434080-T-C

100109208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137433853-G-A

http://identifiers.org/hco/4/GRCh38#100109355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137433731-A-C

100109463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137433626-C-G

http://identifiers.org/hco/4/GRCh38#100109547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137433542-C-A

100109825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137432632-C-T

100109885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137432581-G-A

100109951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137432510-T-C

100109990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137429096-T-C

100109997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137429089-G-A

100110019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137429070-G-A

100110156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137428870-G-A

100110160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137428866-C-T

100110273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137428770-G-A

100110273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137428770-G-C

100110324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137428740-G-A

100110435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137428619-G-T

http://identifiers.org/hco/4/GRCh38#100110570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137428539-A-C

http://identifiers.org/hco/4/GRCh38#100112943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137423072-A-C

100112983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137423033-A-G

100113020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137422996-A-T

100113116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137422891-C-G

100113116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137422891-C-T

100113134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137422873-G-A

100113581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137422463-C-T

100113598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137422446-A-G

100115082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421977-A-G

100115176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421893-G-A

100115209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421860-C-T

100115222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421849-C-G

100115277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421792-G-A

100115451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421658-C-T

100115539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137421601-A-G

100115770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137420530-T-C

100115782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137420518-C-G

100115787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137420512-T-C

http://identifiers.org/hco/4/GRCh38#100115788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137420511-C-A

100115949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137420362-A-G

100116132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137420187-C-T

100117089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137419216-G-A

100117089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137419216-G-T

100117668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418920-G-A

100117668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418920-G-C

100117675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418913-C-G

100117743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418859-G-A

100117743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418859-G-C

100117871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418747-A-G

100117888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418730-T-G

100118749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137418624-T-A

100121481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137416245-G-C

100121511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137416215-A-G

100121874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137415859-T-G

http://identifiers.org/hco/4/GRCh38#100122752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137414906-C-A

http://identifiers.org/hco/4/GRCh38#100122757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137414896-A-C

100122873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137414743-T-A

100122984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137414650-T-C

100123005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137414636-T-A

100123009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137414632-G-A

http://identifiers.org/hco/4/GRCh38#100123335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137410325-C-A

100123481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137410182-T-G

100123539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137410126-A-G

100123739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137409957-A-G

100123776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137409918-C-G

100123776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137409918-C-T

100123864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137409844-T-C

http://identifiers.org/hco/4/GRCh38#100123988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137409726-C-A

100124250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137407470-T-A

100124277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137407439-G-A

100124384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137407329-T-G

100124685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137407106-T-G

100125079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137406459-T-C

100126586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137402757-G-A

100126599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137402744-A-G

100126996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137402289-T-A

100127043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137402248-T-C

100127125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137402172-A-G

100127270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137402010-C-T

http://identifiers.org/hco/4/GRCh38#100127547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137401708-C-A

100127621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137401628-C-T

100128453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137401242-A-T

100128534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137401165-C-T

100128596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137401100-T-C

http://identifiers.org/hco/4/GRCh38#100128661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137401039-C-A

100129774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137400809-T-G

100129790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137400793-T-C

http://identifiers.org/hco/4/GRCh38#100129901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137399822-A-C

100130055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399753-G-C

100130131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399698-G-A

100130434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399339-T-C

100130434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399339-T-G

100130494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399272-C-G

100130494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399272-C-T

100130554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399205-C-T

100130725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137399030-T-C

100130757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398986-A-G

100130773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398970-T-A

100130773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398970-T-C

100130789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398957-A-G

100130907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398842-T-C

100130995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398690-C-G

100131035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398639-G-C

100131239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398374-T-G

100131359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137398255-C-T

100132269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137397418-G-C

100132482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137396869-T-G

100147034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137386793-C-T

100147056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137386771-T-G

http://identifiers.org/hco/4/GRCh38#100147723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137385923-C-A

100147743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137385903-T-C

100148044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137385552-G-A

100148044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137385552-G-T

100148144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137385418-C-T

100148672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137363969-C-G

100148750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137363886-G-A

100150605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137363395-A-G

100150838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137363198-T-C

100151239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137361575-A-G

100151266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137361548-G-A

100151350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137361469-G-C

100151536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137361312-T-C

100152406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137360132-A-G

100157318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137358039-G-C

http://identifiers.org/hco/4/GRCh38#100157701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137357714-C-A

100157701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137357714-C-T

100157727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137357687-A-G

100157846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137357566-T-C

100159753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137356044-G-C

100159917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355883-A-G

100160021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355798-T-C

100160201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355399-T-C

100160306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355299-C-T

100160469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355159-T-G

100160545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355094-T-C

100160605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355035-T-C

100160605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137355035-T-G

http://identifiers.org/hco/4/GRCh38#100160998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137354412-C-A

100161251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137354168-C-G

http://identifiers.org/hco/4/GRCh38#100161315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137354109-A-C

100161390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137354037-A-G

100161398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137354029-A-G

100161484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353950-T-C

100161534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353901-A-G

100161763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353681-G-A

100161819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353627-C-G

100161858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353589-G-A

100161972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353478-A-T

100162024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353436-C-T

100162039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353426-C-T

100162099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353366-A-T

100163100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137353059-G-A

http://identifiers.org/hco/4/GRCh38#100163197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137352974-A-C

100163695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137351458-G-A

100163853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137351340-T-G

http://identifiers.org/hco/4/GRCh38#100163897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137351296-A-C

100164077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137351119-G-A

100164356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137350852-T-A

100165226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137348520-G-C

100165262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137348486-C-T

100166009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137347718-A-G

100166242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137347472-G-C

100166247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137347467-T-C

100166573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137347161-G-A

100166573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137347161-G-T

100167250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137346586-G-T

100167342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137346495-T-C

100167349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137346488-A-G

100167384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137346453-T-C

100167391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137346446-C-T

100167478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345982-A-G

100167523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345944-A-G

100167742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345748-A-G

100167857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345640-C-T

100167873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345624-G-A

100167915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345584-C-T

100167953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345547-G-C

100167960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345540-G-T

100167966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345534-T-A

100168019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345483-G-A

100168056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345447-T-C

100168082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345421-G-C

100168082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137345421-G-T

http://identifiers.org/hco/4/GRCh38#100168156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137345351-C-A

http://identifiers.org/hco/4/GRCh38#100169011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137343203-C-A

100169011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137343203-C-T

100169072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137343141-C-G

100169154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137343073-G-A

100169208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137343024-C-G

100169239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137342987-C-G

100169407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137342172-G-C

100169414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137342165-G-T

100169554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137340150-A-G

http://identifiers.org/hco/4/GRCh38#100169555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137340149-C-A

100169555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137340149-C-T

100169598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137340109-G-A

100169711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137340004-A-T

http://identifiers.org/hco/4/GRCh38#100169792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137339924-C-A

100169872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137339809-T-C

100169941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137339741-T-C

100170067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137339620-G-A

100170067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137339620-G-T

100185976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137334001-T-A

http://identifiers.org/hco/4/GRCh38#100186034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333952-C-A

100186034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333952-C-G

http://identifiers.org/hco/4/GRCh38#100186052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333926-C-A

100186052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333926-C-G

100186052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333926-C-T

100186086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333901-G-C

100186086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333901-G-T

100186114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333870-A-G

100186117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333867-A-G

100186135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333849-A-G

100186135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333849-A-T

100186139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333845-T-G

100186147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333835-G-A

100186164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333818-T-C

100186176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333806-T-C

100186238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333764-T-C

100186252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333750-T-C

100186340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333661-A-G

http://identifiers.org/hco/4/GRCh38#100186362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333639-C-A

http://identifiers.org/hco/4/GRCh38#100186382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333620-A-C

100186429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333578-G-T

100186533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333472-G-T

100186562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333442-A-G

100186658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333341-A-G

http://identifiers.org/hco/4/GRCh38#100186727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333296-C-A

http://identifiers.org/hco/4/GRCh38#100186844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333180-C-A

100186844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137333180-C-T

http://identifiers.org/hco/4/GRCh38#100186903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137333122-C-A

100187265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332743-T-C

100187265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332743-T-G

100187290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332632-A-G

http://identifiers.org/hco/4/GRCh38#100187292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137332630-C-A

100187292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332630-C-G

100187294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332628-T-A

100187294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332628-T-G

100187321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332558-A-T

100187392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332494-A-T

100187534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332354-T-C

100187570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332318-G-T

100187784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332108-G-A

100187784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137332108-G-C

100187929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137331963-C-T

http://identifiers.org/hco/4/GRCh38#100187980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137331912-C-A

100188122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137331770-T-C

100188218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137331683-T-A

100188218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137331683-T-G

100188399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137331510-A-G

100188513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137331407-A-G

100188623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137331295-G-A

100188623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137331295-G-T

100189149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330768-G-C

100189149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330768-G-T

http://identifiers.org/hco/4/GRCh38#100189155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137330762-A-C

100189446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330489-G-A

100189531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330408-G-A

100189686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330231-G-C

100189798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330136-T-C

100189824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137330099-C-T

100189919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137330006-C-T

100189921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137330004-A-G

100189927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329998-C-T

100190183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329749-G-A

100190183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329749-G-C

100190192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329740-G-A

http://identifiers.org/hco/4/GRCh38#100190209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137329723-A-C

100190209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329723-A-T

http://identifiers.org/hco/4/GRCh38#100190303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137329642-C-A

100190303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 137329642-C-G

100190303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 137329642-C-T

100190332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329625-T-G

100190354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329603-A-T

http://identifiers.org/hco/4/GRCh38#100190444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137329519-C-A

100190444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329519-C-T

100190543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137329421-T-A

100190543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137329421-T-C

100190543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137329421-T-G

http://identifiers.org/hco/4/GRCh38#100190544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137329420-C-A

100190637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329329-G-A

100190659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329307-A-G

100190674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329292-A-G

100190674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329292-A-T

100190693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329271-T-C

http://identifiers.org/hco/4/GRCh38#100190707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137329246-C-A

100190707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329246-C-T

100190716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137329237-G-A

100191329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137328650-T-G

100191600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137328376-G-C

100192115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137327940-G-T

100192465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137327608-G-A

http://identifiers.org/hco/4/GRCh38#100192672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137326915-A-C

100192672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137326915-A-G

100192958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137326656-T-C

100193258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137326415-T-C

100193644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137325788-G-T

100193693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137325768-T-G

100193841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137325619-A-G

100194614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137324694-C-T

100194703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137324609-A-T

http://identifiers.org/hco/4/GRCh38#100194838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137324486-A-C

100195021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137324295-G-A

100195021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137324295-G-T