111913185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33728526-G-C

111913185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33728526-G-T

111913578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33728865-A-G

111913590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33728877-C-T

111913656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33728937-G-T

http://identifiers.org/hco/5/GRCh38#111913691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33728957-A-C

111913755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729019-C-G

111913941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729177-C-T

111914002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729238-G-A

111914031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729266-A-T

111914145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729388-A-T

111914752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729413-G-A

111914752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729413-G-T

111914802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729461-T-G

111914878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729535-C-T

111914898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729556-G-A

111914898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729556-G-C

111914942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729598-G-T

http://identifiers.org/hco/5/GRCh38#111914976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33729624-C-A

111915099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729727-G-A

111915125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729752-G-T

111915240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729849-G-A

111915240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33729849-G-C

111915452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33730084-G-A

http://identifiers.org/hco/5/GRCh38#111915607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33730746-C-A

111915607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33730746-C-T

111915639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33730774-T-C

111915644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33730779-C-T

111915647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33730783-G-A

111915719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33730828-T-C

111916371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33731706-C-T

111916657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33731946-T-C

111916694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33731980-G-A

111916750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33732036-G-C

111916766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33732052-T-G

111928917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33733701-T-G

111929010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33733794-G-A

111929436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734211-A-G

111929493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734267-A-G

111929852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734623-C-T

111929867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734638-C-T

111929921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734690-G-T

111930061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734822-G-T

111930108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734869-G-T

111930115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33734876-G-A

111930196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33734950-A-G

111930307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735049-C-T

111930346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735088-C-G

111930406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735152-T-A

111930493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735229-G-C

111930519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735255-C-T

111930850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735565-C-G

111930957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735671-C-T

111931108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33735753-C-G

111931118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33735763-T-C

111931118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33735763-T-G

111931149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33735794-G-A

111931255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33735887-C-T

111931272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33735904-A-G

111931414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33736041-G-A

111931414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33736041-G-T

http://identifiers.org/hco/5/GRCh38#111931577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33736258-C-A

111931578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33736259-C-T

111931742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33736938-G-A

http://identifiers.org/hco/5/GRCh38#111932035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33737212-C-A

111932092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737265-T-A

111932092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737265-T-C

http://identifiers.org/hco/5/GRCh38#111932185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33737330-A-C

111932258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737400-G-A

111932270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737412-T-C

111932394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737533-A-G

111932403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737542-T-C

111932408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737547-C-T

111932578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33737724-T-A

111932787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738132-G-A

111932981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738288-G-A

111933108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738389-C-T

111933175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738453-A-G

111933187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738465-C-G

111933263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738534-A-G

111933470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738731-G-A

111933575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738835-G-A

http://identifiers.org/hco/5/GRCh38#111933629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33738889-A-C

111933643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738904-C-G

111933643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33738904-C-T

111934613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33739293-G-C

111934642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33739322-G-A

111934715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33739394-A-G

111934825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33739505-G-T

111937323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33741723-T-A

111937500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33741877-C-T

111937510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33741889-C-G

111937588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33741994-A-T

111937653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742056-C-T

111937715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742119-G-A

111937914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742214-C-T

111938002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742286-G-A

111938002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742286-G-T

111938158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742430-G-A

111938214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742482-C-T

111938339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33742614-A-G

111938597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33746402-G-A

111938610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33746415-C-T

111938636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33746440-G-A

111938659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33746457-A-G

111938808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33746624-C-T

http://identifiers.org/hco/5/GRCh38#111940949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33747590-A-C

111940949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747590-A-T

111940998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747642-T-C

111941024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747668-G-A

111941079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747708-A-G

111941079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747708-A-T

111941162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747794-G-A

111941259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747882-G-C

111941322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33747941-T-G

111941412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33748029-G-A

111941569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33748215-T-A

111941579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33748225-G-C

111941825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33749438-A-T

111941832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33749445-A-G

111942883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33750470-G-A

111942919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33750516-G-A

111942919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33750516-G-T

111943431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33750954-C-T

111943477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751005-T-G

111943513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751041-G-C

111943513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751041-G-T

111943521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751049-G-T

http://identifiers.org/hco/5/GRCh38#111943546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33751073-A-C

111943587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751108-T-C

http://identifiers.org/hco/5/GRCh38#111943640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33751156-C-A

111943773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751269-T-C

111943776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751272-T-A

111943907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751397-T-C

111944990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33751863-A-G

http://identifiers.org/hco/5/GRCh38#111945049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33752051-A-C

111945111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752115-C-T

111945115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752119-C-G

http://identifiers.org/hco/5/GRCh38#111945436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33752461-C-A

111945523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752527-G-A

111945523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752527-G-T

111945540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752537-T-G

111945700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752665-G-A

111945700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752665-G-C

111945704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752669-A-G

111945828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33752785-G-A

111946113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33753250-A-T

http://identifiers.org/hco/5/GRCh38#111946121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33753258-C-A

111946121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33753258-C-T

111946202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33753344-T-C

111946258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33753978-T-G

111946553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33754212-T-A

111946607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33754286-G-C

111946841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33754556-C-G

111946841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33754556-C-T

111946907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33754634-C-T

http://identifiers.org/hco/5/GRCh38#111947774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33755672-A-C

111948552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33756437-T-C

111948584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33756466-C-G

111948826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33756721-T-A

111951128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33757566-T-C

111951743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33757940-C-T

111952005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758193-C-T

111952194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758348-C-G

http://identifiers.org/hco/5/GRCh38#111952228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33758382-A-C

111952274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758425-C-T

111952290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758441-G-A

http://identifiers.org/hco/5/GRCh38#111952467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33758605-C-A

111952467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758605-C-T

111952511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758620-C-T

111952530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33758639-C-T

111953286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33759067-G-A

111953287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33759068-T-C

111953598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33759373-T-G

111961459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33759956-T-C

111961459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33759956-T-G

111961612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33760089-G-T

http://identifiers.org/hco/5/GRCh38#111961778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33760251-C-A

111961778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33760251-C-G

111961934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33760420-T-C

111966026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33767987-A-T

http://identifiers.org/hco/5/GRCh38#111966057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33768017-C-A

111966057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33768017-C-T

111966081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33768039-A-G

111966176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33768125-G-T

111966215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33768154-G-A

111966352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33774724-C-T

111966534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33774901-G-A

111966637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775002-A-G

http://identifiers.org/hco/5/GRCh38#111966816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33775141-A-C

111966854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775209-A-G

http://identifiers.org/hco/5/GRCh38#111966870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33775227-A-C

111966947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775293-A-G

111967292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775736-A-G

http://identifiers.org/hco/5/GRCh38#111967568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33775972-C-A

111967581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775985-A-G

111967581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775985-A-T

111967590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33775993-G-A

111967600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33776003-T-C

111968110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33776420-A-G

111968238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33776553-G-C

111968391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33776702-G-A

111976037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783377-T-C

111976271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783601-T-C

111976345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783675-G-A

111976459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783774-G-C

http://identifiers.org/hco/5/GRCh38#111976493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33783810-A-C

111976622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783930-G-C

111976622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783930-G-T

111976664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33783980-A-G

http://identifiers.org/hco/5/GRCh38#111976738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33784043-A-C

111976738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784043-A-G

111976738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784043-A-T

http://identifiers.org/hco/5/GRCh38#111976793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33784094-C-A

http://identifiers.org/hco/5/GRCh38#111976801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33784102-C-A

111976801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784102-C-G

111976801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784102-C-T

111976828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784129-C-G

111976842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784143-A-G

111976883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784185-G-A

111976883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784185-G-T

111976902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33784204-T-C

111976958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33784268-G-T

111976968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33784278-T-A

111977208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33784506-A-T

111977231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33784529-T-C

111977278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33784575-A-G

111979449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33788718-C-G

111981383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789109-C-T

111981400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789126-C-T

111981432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789160-T-C

111981434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789162-G-A

111981434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789162-G-C

http://identifiers.org/hco/5/GRCh38#111982068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33789819-C-A

111982068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789819-C-T

111982079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789830-T-A

111982079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789830-T-C

111982116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789890-G-A

111982116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789890-G-C

111982116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789890-G-T

111982120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789891-G-C

111982137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789908-C-T

111982154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33789937-C-T

111982299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33790072-T-C

111982462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33790235-G-A

111982533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33790299-T-C

111982561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33790331-G-A

111982572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33790342-G-C

111982646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33790415-T-C

111982909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791313-G-A

111983007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791400-T-C

111983192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791560-C-G

111983192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791560-C-T

111983194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791562-A-G

111983234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791599-G-A

http://identifiers.org/hco/5/GRCh38#111983235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33791600-C-A

http://identifiers.org/hco/5/GRCh38#111983269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33791675-A-C

111983467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33791976-T-C

111983563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33792062-G-A

111983959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33792571-A-G

111984326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33792946-G-A

111984334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33792951-T-A

111984334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33792951-T-C

111984334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33792951-T-G

111984411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33793028-G-T

111984489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33793097-T-C

111984616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33793249-C-T

http://identifiers.org/hco/5/GRCh38#111984878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33794085-C-A

111984975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33794159-A-G

111984975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33794159-A-T

111985501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33794661-T-A

111985650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33795243-A-G

111985710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33795299-A-T

111992433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796417-C-T

111992624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796564-T-A

111992667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796605-C-G

111992667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796605-C-T

111992785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796726-G-A

111992785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796726-G-C

111992819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796758-G-A

111993206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796947-G-A

111993253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33796984-G-A

http://identifiers.org/hco/5/GRCh38#111993350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33797065-C-A

http://identifiers.org/hco/5/GRCh38#111993492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33797197-C-A

111993530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33797226-A-G

111995929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33797871-G-A

111995936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33797878-G-A

111996102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798017-C-T

111996104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798019-T-C

111996111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798026-C-T

111996123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798035-A-T

111996195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798112-T-C

111996351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798252-C-G

111996372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798273-T-A

111996372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798273-T-C

111996594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798486-A-G

111996625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798517-G-A

http://identifiers.org/hco/5/GRCh38#111996629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33798521-A-C

111996629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33798521-A-G

http://identifiers.org/hco/5/GRCh38#111996648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33798540-A-C

111996776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799290-A-G

111996791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799305-C-G

111996806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799321-A-T

111996874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799389-G-T

111996926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799438-G-T

111997083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799571-G-A

111997083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799571-G-C

111997185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799668-T-C

111997203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799686-T-C

111997204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799687-G-T

111997220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799701-C-G

111997241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799722-T-C

111997276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799758-G-T

111997295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33799784-T-C

http://identifiers.org/hco/5/GRCh38#111997327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33799820-C-A

111997327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33799820-C-T

111997348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33799840-G-C

111997348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33799840-G-T

111997437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33799921-C-T

111997506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33799989-T-C

111997507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33799990-G-C

111997758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33800192-G-A

http://identifiers.org/hco/5/GRCh38#111997769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33800196-C-A

111997909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33800345-A-T

111998009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33800469-G-C

111998009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33800469-G-T

111998139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33800610-T-C

111998231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33800703-T-C

111998256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33800719-T-C

111998288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33800751-A-T

111998355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33800837-C-T

111998366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33800848-C-T

111998540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801101-A-T

111998560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801124-T-C

111998562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801126-T-G

111998569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801148-C-T

111998581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801160-T-C

111998704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801311-A-G

111998846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801502-G-T

111998917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801611-A-G

111998955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801661-C-T

111999040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33801741-G-C

112000241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803116-T-A

112000370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803243-C-T

112000548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803418-A-G

http://identifiers.org/hco/5/GRCh38#112000567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33803439-A-C

112000707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803578-T-A

112000707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803578-T-C

112000738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803600-C-T

112000743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803605-C-T

112001112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803848-G-C

112001211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33803943-G-A

112001326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33804062-C-T

112001392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33804190-C-T

112001512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33804311-G-A

http://identifiers.org/hco/5/GRCh38#112002497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33805232-A-C

112002525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33805259-G-A

112002525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33805259-G-C

http://identifiers.org/hco/5/GRCh38#112002588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33805322-A-C

112002588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33805322-A-G

112002980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33805603-C-T

112003049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33805672-G-A

112003069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33805685-C-T

112003268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806148-A-G

112003399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806299-C-T

112003464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806372-T-C

112003649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806548-T-C

http://identifiers.org/hco/5/GRCh38#112003659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33806558-C-A

112003659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806558-C-G

http://identifiers.org/hco/5/GRCh38#112003697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33806582-C-A

112003747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806630-C-T

112003906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806751-A-T

http://identifiers.org/hco/5/GRCh38#112003959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33806806-C-A

112003959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33806806-C-G

112004804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33807295-G-C

112004857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33807348-A-G

112004942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33807430-T-C

112004972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33807458-A-G

112005071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33807556-G-C

http://identifiers.org/hco/5/GRCh38#112005079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#33807564-C-A

112005079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33807564-C-T

112005128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33807613-G-A

112005501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33807916-C-T

112005850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33808260-G-A

112006114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33808497-G-A

112006377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33808768-C-T

http://identifiers.org/hco/5/GRCh38#112006460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33808847-C-A

112006571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33808951-G-A

112006590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33808979-C-G

http://identifiers.org/hco/5/GRCh38#112006608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33809003-A-C

112006610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33809005-C-T

http://identifiers.org/hco/5/GRCh38#112007105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33816282-A-C

http://identifiers.org/hco/5/GRCh38#112009275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33817986-C-A

112009279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33817990-T-A

http://identifiers.org/hco/5/GRCh38#112009294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33818005-C-A

112009294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33818005-C-G

112009316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33818030-A-G

112010539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33819732-G-A

112010963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33820089-A-G

112011046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33820166-G-A

112011046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33820166-G-T

112011224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33820339-T-C

112011230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33820361-T-G

112012443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33825368-C-T

112012467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33825396-A-T

112012655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33825811-T-C

112012670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33825826-C-G

112013079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33826233-G-A

112013113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33826271-A-T

112013200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33826360-A-G

112013441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33828839-G-A

112013449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33828847-C-T

112013924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33829243-G-C

112014092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33829403-G-T

112014414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33829706-T-C

http://identifiers.org/hco/5/GRCh38#112014461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33829749-A-C

112014922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33830207-C-T

112015069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33830349-G-A

112015252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837312-T-C

112015257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837317-G-A

112015349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837409-A-G

112015360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837420-T-C

112015365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837425-A-G

http://identifiers.org/hco/5/GRCh38#112015452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33837507-C-A

http://identifiers.org/hco/5/GRCh38#112015467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33837520-A-C

112015528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837579-T-G

112015661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837692-C-G

112015661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33837692-C-T

112016328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33838373-T-C

http://identifiers.org/hco/5/GRCh38#112016586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33838665-A-C

112017145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: non coding transcript exon variant
orthologous variants: 33839649-G-T

112017173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: non coding transcript exon variant
orthologous variants: 33839675-G-T

http://identifiers.org/hco/5/GRCh38#112017200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#33839723-C-A

112017200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40780
most severe consequence: non coding transcript exon variant
orthologous variants: 33839723-C-T