2907075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27460044-A-G

2907119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27460088-G-A

2907123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27460092-G-C

2907124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27460093-G-A

2907124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27460093-G-C

2907132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27461010-A-G

2907132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27461010-A-T

2907136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27461014-C-T

http://identifiers.org/hco/9/GRCh38#2907212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27461090-C-A

2907212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461090-C-T

2907233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461114-A-T

http://identifiers.org/hco/9/GRCh38#2907237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27461118-C-A

2907237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461118-C-G

2907237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461118-C-T

http://identifiers.org/hco/9/GRCh38#2907274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27461145-C-A

2907700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461536-G-C

2907851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461692-A-G

2907857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461698-C-T

2907860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461701-T-C

2907881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461722-A-G

2907943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461775-A-T

2907953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461785-G-A

2908144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461933-C-T

2908164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461953-A-G

2908164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461953-A-T

2908206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27461999-A-T

http://identifiers.org/hco/9/GRCh38#2908207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27462000-C-A

2908281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462072-C-T

2908665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462152-T-A

2908885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462336-G-A

2908896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462348-G-C

2909024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462711-G-A

2909026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462713-G-A

2909026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462713-G-C

2909046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462733-G-A

2909077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462764-G-A

2909077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462764-G-C

2909077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462764-G-T

2909148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462817-A-G

2909157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27462818-A-T

2909508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466647-C-G

2909569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466696-T-G

http://identifiers.org/hco/9/GRCh38#2909590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27466717-C-A

2909590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466717-C-G

2909660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466771-C-T

2909667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466778-C-T

http://identifiers.org/hco/9/GRCh38#2909732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27466836-C-A

2909732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466836-C-G

2909813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466936-A-T

2909819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27466973-T-A

2909848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467006-T-A

2909928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467086-C-T

2910241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467293-A-T

2910242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467294-G-A

2910242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467294-G-C

2910408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467438-C-T

2910502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467519-T-C

2910580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467592-C-T

2910584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467596-G-A

2910633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467650-G-A

2910653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467670-C-T

2911012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27467949-C-G

http://identifiers.org/hco/9/GRCh38#2911047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27467972-C-A

2911143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468056-T-C

2911267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468174-A-G

2911519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468431-G-A

2911519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468431-G-C

2911536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468442-T-C

http://identifiers.org/hco/9/GRCh38#2911666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27468496-C-A

2911666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468496-C-T

2911693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468523-T-C

2911751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468583-T-C

2911758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468590-G-T

2911944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468777-C-T

2911951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468784-A-G

2911992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468825-T-C

2912137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27468983-G-A

2912272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27469097-G-A

2912428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27469250-T-A

2912872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27469715-A-T

http://identifiers.org/hco/9/GRCh38#2914200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27475725-C-A

2914342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27475892-T-A

2914455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27475986-T-C

2914655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27476160-T-C

2914924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27476433-C-T

2917478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479544-G-C

2917571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479621-C-T

2917801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479830-C-T

2917804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479833-A-T

2917813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479842-G-A

2917880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479908-C-T

2918061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27479989-G-T

http://identifiers.org/hco/9/GRCh38#2918419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27480251-A-C

2918419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480251-A-T

2918453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480283-C-T

http://identifiers.org/hco/9/GRCh38#2918521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27480320-C-A

2918615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480407-G-A

2918666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480465-C-T

2918680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480477-C-T

2918750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480544-T-C

2918750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480544-T-G

2918827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480623-C-T

2918886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480680-G-A

http://identifiers.org/hco/9/GRCh38#2918929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27480701-C-A

2918929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480701-C-G

2918943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480715-A-T

2918951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480723-G-A

2919050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27480823-A-G

2919178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27480966-A-G

http://identifiers.org/hco/9/GRCh38#2919262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27481037-C-A

2919262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27481037-C-T

2919319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27481069-G-T

2919530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481292-C-G

2919683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481443-T-C

2919790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481576-G-A

2919790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481576-G-T

2919830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481617-T-G

2919931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481717-G-T

2920003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481791-C-G

2920007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481795-T-C

2920048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481821-C-T

2920078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481850-A-G

2920090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481862-T-C

2920112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481888-T-C

2920207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481961-G-T

2920209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27481963-A-G

2920304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482058-T-A

2920374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482121-C-T

2920412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482482-G-A

2920412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482482-G-C

2920421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482524-C-T

2920458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482567-A-G

2920496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482605-C-T

2920512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482621-T-C

2920560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482669-G-A

2920560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482669-G-C

2920596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482701-G-T

2920629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482731-G-T

2920659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482755-G-A

http://identifiers.org/hco/9/GRCh38#2920673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27482769-A-C

2920678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482774-C-T

http://identifiers.org/hco/9/GRCh38#2920686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27482782-C-A

2920901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482936-T-C

2920938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482971-G-A

2920938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482971-G-T

2920953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27482986-T-C

2921040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27483079-C-T

2921383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27483396-G-C

2921422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27483433-C-T

2921460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27483442-G-C

2921534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27483520-T-A

2921547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27483533-C-T

2921782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 27484001-C-T

2921792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484011-T-C

2921792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484011-T-G

2921834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484046-T-A

2921834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484046-T-G

2921835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484047-T-C

2921835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484047-T-G

2921841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484053-T-A

2921869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484081-T-G

2921870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484082-G-A

2921870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27484082-G-T

2921919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484131-C-T

2922419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484355-G-C

2922476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484402-G-A

2922476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484402-G-C

2922489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484415-C-T

2922522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484446-G-C

2922593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484499-T-G

2922614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484520-C-G

2922616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484522-G-A

2922767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484668-C-T

2922794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484695-G-A

2922872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484771-T-C

2922906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484804-T-C

2922915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484813-T-G

2923015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484917-T-C

2923048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484949-T-C

2923056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484957-T-C

2923062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27484963-A-G

2923980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485119-C-T

2924000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485139-C-T

2924145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485285-G-A

http://identifiers.org/hco/9/GRCh38#2924178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27485318-C-A

2924178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485318-C-T

http://identifiers.org/hco/9/GRCh38#2924187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27485327-C-A

2924197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485337-C-T

2924234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485374-C-T

http://identifiers.org/hco/9/GRCh38#2924247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27485387-C-A

http://identifiers.org/hco/9/GRCh38#2924263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27485405-C-A

2924263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485405-C-T

2924265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485407-C-T

2924450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485511-C-G

2924450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485511-C-T

2924667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485712-T-C

2924725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485766-T-C

2924725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485766-T-G

2924908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27485949-T-C

2925024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486074-A-G

2925024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486074-A-T

2925135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486183-C-G

2925135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486183-C-T

2925154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486197-C-G

2925275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486314-C-G

2927751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486683-T-C

2927860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486790-T-C

2927899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486829-C-T

http://identifiers.org/hco/9/GRCh38#2927926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27486856-C-A

2927926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486856-C-G

2927926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486856-C-T

http://identifiers.org/hco/9/GRCh38#2927974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27486907-A-C

2927974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27486907-A-G

2928196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487068-G-A

2928217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487089-G-A

2928285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487155-G-A

2928325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487208-A-T

2928331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487214-G-T

2928345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487228-C-G

2928358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487241-G-C

2928411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487298-T-C

2928422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487309-G-T

2928478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487342-C-T

2929062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487910-T-C

2929089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27487944-T-C

2929222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27488755-G-C

2929312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27488856-G-A

2929479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27488963-T-G

2931422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27490795-T-C

2931552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27490904-T-A

2931601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27490949-C-T

2931738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27491090-A-T

2932058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27491599-C-T

2932272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27491807-C-T

2932394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27491923-A-G

2932657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492183-C-G

2932657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492183-C-T

http://identifiers.org/hco/9/GRCh38#2932779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27492308-C-A

2932815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492344-A-T

2932817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492346-G-A

2932855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492358-G-A

2932944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492458-G-A

2932996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492509-T-C

2933012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492533-T-G

2935788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27492924-A-G

2935912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493048-G-C

http://identifiers.org/hco/9/GRCh38#2935920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27493056-C-A

2935936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493078-C-T

2936021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493149-A-G

2936040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493164-T-A

2936215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493292-G-A

http://identifiers.org/hco/9/GRCh38#2936358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27493458-C-A

2936470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493551-A-G

2936655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493733-C-T

2936729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493776-T-C

2936777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493811-G-C

2936828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493847-G-A

2936914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27493963-G-C

2937110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494166-G-C

2937139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494195-A-T

2937341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494395-T-C

2937413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494472-G-A

http://identifiers.org/hco/9/GRCh38#2937571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27494627-A-C

2937698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494750-C-T

2937740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494792-G-T

2937781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27494813-T-A

2938504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27495821-G-A

2938558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27495871-G-A

2938730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27496041-T-C

2938731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27496042-G-C

2938739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27496050-G-C

2939058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27496889-G-A

2939134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27496951-A-G

2939618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27497405-A-G

2939618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27497405-A-T

2939697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27497462-G-A

2939729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27497496-C-T

2939768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27497534-G-T

2939789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27497556-G-A

2940315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27498091-T-A

2940375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27498152-C-G

2940484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27498263-G-A

http://identifiers.org/hco/9/GRCh38#2940654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27498442-C-A

2940960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27498762-G-A

2942491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27499658-C-G

2942509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27499640-C-T

2942866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27500625-G-C

2942880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27500638-T-C

2943024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27500774-C-T

2943491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27501241-T-A

2943638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27501393-A-G

2943650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27501406-T-C

2943650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: non coding transcript exon variant
orthologous variants: 27501406-T-G

2943738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27501495-C-T

2943911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502005-C-T

2943934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502025-C-G

2943934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502025-C-T

2943953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502046-C-T

2944045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502145-C-T

2944159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502242-A-G

2944430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502483-G-T

2944443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502494-C-T

2944480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502530-T-A

2944606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502663-G-A

http://identifiers.org/hco/9/GRCh38#2944652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27502709-C-A

2944701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502754-C-G

2944792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27502847-T-C

2944950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27503010-G-A

2944950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27503010-G-T

2944970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27503055-T-C

2945791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504032-A-G

2945959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504189-T-C

2945968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504198-A-G

http://identifiers.org/hco/9/GRCh38#2946025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27504259-C-A

2946055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504290-G-A

2946055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504290-G-T

http://identifiers.org/hco/9/GRCh38#2946070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27504304-C-A

2946070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504304-C-G

2946125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504359-A-G

http://identifiers.org/hco/9/GRCh38#2946134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27504369-C-A

2946143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504378-A-G

2946163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504398-C-G

2946185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504411-T-C

2946241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504467-G-C

2946380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504599-T-C

2946380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504599-T-G

2946399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504616-C-T

2946425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504654-A-T

2946607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504890-C-T

2946617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504900-T-A

2946617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504900-T-C

2946676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27504962-C-G

2946726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27505012-C-T

2946818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27505090-A-G

2946853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27505118-C-T

http://identifiers.org/hco/9/GRCh38#2947035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27505327-A-C

2947960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27507970-G-T

2948442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27508841-C-T

2948515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27508914-T-C

http://identifiers.org/hco/9/GRCh38#2948627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27508978-A-C

2948630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27508981-T-C

2948680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27509033-C-T

2957196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27512284-C-T

2957354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27512424-C-G

2957380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27512450-T-A

2957380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27512450-T-C

2958140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27512671-T-C

2958229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27512760-G-A

2958558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513090-T-C

2958647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513570-T-C

2958647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513570-T-G

2958880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513793-C-G

2958903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513824-C-G

2959029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513937-T-C

2959075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27513980-C-G

2959100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514005-T-A

2959310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514481-T-A

2959311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514482-C-T

2959384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514571-G-A

2959415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514601-C-T

2959581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514761-A-G

http://identifiers.org/hco/9/GRCh38#2959720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27514882-C-A

2959720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514882-C-T

2959766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27514927-G-C

2959909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515063-T-C

2959932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515093-G-T

2960060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515215-A-G

2960109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515267-C-G

http://identifiers.org/hco/9/GRCh38#2960162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27515320-A-C

2960185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515343-G-C

http://identifiers.org/hco/9/GRCh38#2960300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27515443-C-A

2960947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515712-G-A

2961034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515791-T-C

2961103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27515801-A-G

2961466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27516081-G-A

2961495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27516109-G-A

2961495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27516109-G-T

2961530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27516134-T-C

2961558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27516162-A-T

2961660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27516442-C-T

2961940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517393-G-A

2962068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517525-C-T

2962150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517606-G-A

2962290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517740-G-T

2962324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517770-C-T

2962357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517806-C-T

2962583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517940-T-C

2962646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27517995-A-G

2962860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518207-T-C

2963031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518370-A-G

2963141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518480-C-T

2963168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518522-C-G

2963168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518522-C-T

2963195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518560-A-G

2963267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518617-C-G

2963507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27518843-G-A

2963750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519079-G-C

2963907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519240-A-G

2963959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519288-G-A

2964042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519372-G-C

2964230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519553-C-T

http://identifiers.org/hco/9/GRCh38#2964254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27519577-C-A

2964254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519577-C-T

http://identifiers.org/hco/9/GRCh38#2964267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27519590-A-C

2964416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519729-T-G

2964420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519733-G-A

2964683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27519981-G-C

2966633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27522364-C-G

2966947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524011-C-T

2967267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524325-G-C

2967296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524356-G-A

2967717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27524752-G-A

2979302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532214-A-G

2979336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532248-C-G

2979337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532249-A-G

2979711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532603-A-G

http://identifiers.org/hco/9/GRCh38#2979756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27532640-A-C

2979811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532720-C-G

2979895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27532802-G-A

2980235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533119-C-G

2980281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533165-C-T

2980302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533186-G-A

2980503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533366-A-G

2980555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27533418-G-C

2981999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27534248-A-G

http://identifiers.org/hco/9/GRCh38#2982058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27534307-C-A

2982058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27534307-C-T

2982455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27534681-G-A

2984702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535813-T-C

2984766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27535886-A-T

http://identifiers.org/hco/9/GRCh38#2984767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27535887-C-A

http://identifiers.org/hco/9/GRCh38#2985013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27536132-C-A

2985013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536132-C-G

http://identifiers.org/hco/9/GRCh38#2985199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27536354-A-C

2985199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536354-A-G

2985319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536467-A-G

2985649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27536798-G-C

2985883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539632-A-G

2986042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539781-T-A

2986043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27539782-C-T

2986930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27540263-C-T

2987146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27540467-T-C

2987233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27540552-A-G

2987480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27540808-G-A

http://identifiers.org/hco/9/GRCh38#2987523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27540832-C-A

http://identifiers.org/hco/9/GRCh38#2987532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27540841-A-C

http://identifiers.org/hco/9/GRCh38#2987680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27540989-C-A

2987723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541032-A-G

2987723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541032-A-T

2988090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541361-T-A

2988195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541464-C-G

2988217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541486-C-T

http://identifiers.org/hco/9/GRCh38#2988317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27541567-C-A

2988462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541876-C-T

2988468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541882-A-G

http://identifiers.org/hco/9/GRCh38#2988479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27541893-C-A

2988479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27541893-C-G

2988584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542092-G-T

http://identifiers.org/hco/9/GRCh38#2988667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27542173-A-C

http://identifiers.org/hco/9/GRCh38#2988723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27542234-A-C

2988825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542315-T-C

2989239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542723-T-C

2989262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27542746-T-C

2989346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543031-A-G

2989460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543138-A-G

2989462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543140-G-A

2989462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543140-G-C

2989462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543140-G-T

2989507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543181-G-T

2989744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543367-A-G

2989933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543551-A-G

2989995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27543602-A-G

http://identifiers.org/hco/9/GRCh38#2989998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27543605-C-A

2990370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544072-G-A

2990370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544072-G-T

2990443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544172-A-G

2990460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544182-A-G

2993884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544548-A-G

2994066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544730-C-G

2994227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544860-A-G

2994273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544915-G-A

2994279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544922-T-C

2994284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27544927-A-T

2994401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545042-G-C

2994783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545768-G-C

2994968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27545944-T-C

2995269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546241-T-C

2995269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546241-T-G

2995341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546308-G-A

http://identifiers.org/hco/9/GRCh38#2995445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27546775-C-A

2995445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546775-C-T

2995463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546793-A-G

2995463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546793-A-T

http://identifiers.org/hco/9/GRCh38#2995482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27546812-A-C

2995503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27546830-A-G

2995730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547039-C-G

2995730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547039-C-T

2995865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547625-G-C

http://identifiers.org/hco/9/GRCh38#2995919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27547665-C-A

2995976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547722-G-A

2995976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547722-G-T

2995992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547741-G-A

2995992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547741-G-C

http://identifiers.org/hco/9/GRCh38#2996001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27547750-C-A

http://identifiers.org/hco/9/GRCh38#2996134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27547877-C-A

2996134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547877-C-G

2996200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547955-G-C

2996218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27547973-G-C

2996420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548178-G-A

2996444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548202-C-T

2996453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548211-A-T

2996540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548315-T-C

2996556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548331-G-A

2996564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548339-A-G

2996580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548348-G-C

2996789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548829-C-G

2996906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548941-C-T

2996917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548952-T-C

2996918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27548953-A-T

2997047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27549081-G-A

2997047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27549081-G-C

2997151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27549192-C-G

2998676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550507-A-T

2998809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550624-T-C

2998840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550652-T-C

2998867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550674-C-G

2998875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550681-G-A

2998937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550743-A-T

2998962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550765-T-C

2998975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550769-G-T

2999081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27550891-T-A

2999146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551001-G-A

3000285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551375-T-C

3000326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551416-C-T

3000470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551566-T-C

3000547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551630-G-A

3000656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551729-C-T

3000777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551830-C-G

3000777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551830-C-T

3000820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551870-G-A

3000823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551873-G-T

3000827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551877-T-A

3000827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551877-T-C

3000897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551947-T-C

3000915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551965-T-C

3000916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27551966-T-G

3001094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552174-G-A

http://identifiers.org/hco/9/GRCh38#3001125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27552204-C-A

3001164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552257-T-C

3001501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552906-G-A

3001501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552906-G-C

3001601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552981-T-C

3001603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27552983-G-C

3001705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553069-G-T

3001754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553091-C-G

3001864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553202-T-C

3001928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553260-T-C

3001966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553297-G-A

3002001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553347-G-T

3002178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553578-A-G

3002179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553579-T-A

3002203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553603-G-C

3002276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553676-G-A

3002361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553756-T-A

3002523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553900-C-T

3002568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27553931-A-G

3002664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554032-C-T

3002735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554102-G-C

3002867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554219-A-G

3002867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554219-A-T

3002873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554225-C-T

3003121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554250-T-C

3003151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554280-C-T

http://identifiers.org/hco/9/GRCh38#3003783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27554522-C-A

3003785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554524-T-C

3003785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554524-T-G

3003795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554534-C-T

3003942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554803-A-G

3003975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27554870-T-A

3004172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555076-C-T

3004222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555115-A-G

http://identifiers.org/hco/9/GRCh38#3004247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27555134-C-A

3004247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555134-C-T

3004607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27555457-G-A

3004866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556306-C-T

3004966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556759-T-G

3005091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556856-C-T

3005166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556931-A-G

3005227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556992-G-A

3005227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27556992-G-C

3005384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557147-T-G

3005505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557266-T-C

3005592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27557355-A-G

3005736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558013-T-C

http://identifiers.org/hco/9/GRCh38#3005784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27558057-C-A

3005784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558057-C-G

3005843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558097-G-A

3005843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558097-G-C

3005988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558250-C-G

3005988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558250-C-T

3006043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558331-G-T

3006118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558386-T-A

3006319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558569-A-G

3006644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27558879-C-T

3006823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559059-C-T

3006852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559088-C-T

3006886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559122-G-A

3006906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559143-C-T

3007157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559409-G-A

3007331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559598-C-T

3007504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559804-G-A

http://identifiers.org/hco/9/GRCh38#3007639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27559934-C-A

3007710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27559998-G-A

3007717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560005-A-G

http://identifiers.org/hco/9/GRCh38#3007847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27560148-A-C

3008289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560494-G-A

3008520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27560723-G-A

3008973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561115-A-G

http://identifiers.org/hco/9/GRCh38#3009042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27561200-C-A

3009042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561200-C-T

3009103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561261-G-A

3009133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561291-A-G

http://identifiers.org/hco/9/GRCh38#3009146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27561304-C-A

3009146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561304-C-G

3009146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561304-C-T

3009256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561496-C-G

3009474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561695-T-G

3009497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27561720-C-T

3011375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562413-G-A

3011416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562452-T-C

3011438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562473-G-C

3011525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562549-G-A

3011530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562554-C-G

3011530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562554-C-T

3011651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562649-C-T

3011687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562667-C-G

3011858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562834-A-G

3011950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27562917-A-G

3012070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563039-G-C

3012352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563335-T-C

3012457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563440-C-T

3012518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563496-G-A

http://identifiers.org/hco/9/GRCh38#3012539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27563521-C-A

3012558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563540-T-C

3012871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563779-T-C

3012871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27563779-T-G

3014372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564347-G-A

3014372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564347-G-T

3014539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564139-A-G

3014539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564139-A-T

3014776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564463-G-A

3014819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564503-T-C

3015106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564759-C-T

3015323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564910-G-C

3015323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564910-G-T

3015363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27564939-T-C

3015465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565032-G-A

3016449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565308-A-G

3016508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565358-C-T

3016655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565834-T-A

3016720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565900-G-A

3016747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27565927-T-C

http://identifiers.org/hco/9/GRCh38#3017087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27566209-C-A

3017310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27566431-T-A

3017310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27566431-T-C

3017770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27566566-A-G

3018008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27566800-A-T

3018079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27566852-G-A

3018414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27567163-G-T

3018449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27567191-G-A

3018449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27567191-G-T

3018585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27567343-G-T

3018928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27568481-G-A

3018928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27568481-G-C

http://identifiers.org/hco/9/GRCh38#3019334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27568843-A-C

3019334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27568843-A-G

3019414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27568914-T-C

http://identifiers.org/hco/9/GRCh38#3019513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27569012-C-A

3019513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569012-C-G

3019562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569061-G-A

http://identifiers.org/hco/9/GRCh38#3019589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27569089-C-A

http://identifiers.org/hco/9/GRCh38#3019991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27569427-C-A

3020420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569758-G-A

3020420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569758-G-T

3020563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27569923-A-G

3021667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27570251-G-C

3021730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27570296-T-A

3022214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27570969-A-G

http://identifiers.org/hco/9/GRCh38#3022394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27571146-A-C

http://identifiers.org/hco/9/GRCh38#3022441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27571193-A-C

3022508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27571260-T-A

3022508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27571260-T-C

3022629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27571373-T-C

3022800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27571543-G-A

3023123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572044-G-C

3023130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572051-C-T

3023182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572088-C-T

3023243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572136-T-A

3023243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572136-T-C

3023262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572155-G-A

3023586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572476-G-A

http://identifiers.org/hco/9/GRCh38#3023596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27572857-C-A

3023596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27572857-C-T

3023850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573085-T-C

3023902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573139-G-T

3023951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573188-C-T

3024164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573376-C-T

3024211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573440-C-T

http://identifiers.org/hco/9/GRCh38#3024247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27573482-C-A

3024251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573486-C-T

http://identifiers.org/hco/9/GRCh38#3024264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27573501-C-A

3024298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573530-C-T

3024338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573572-G-A

3024357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573590-G-A

3024810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573959-T-C

3024846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573995-G-A

3024846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27573995-G-C

3024861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574010-C-T

http://identifiers.org/hco/9/GRCh38#3024872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27574021-C-A

3024872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574021-C-T

3024878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574027-G-C

3024878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574027-G-T

3024931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574084-G-A

3024950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574103-G-A

http://identifiers.org/hco/9/GRCh38#3025003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27574154-C-A

http://identifiers.org/hco/9/GRCh38#3025192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27574333-C-A

3025480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574609-G-C

3025598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574724-G-A

3025744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574866-A-G

3025785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574906-A-G

3025860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27574982-G-A

3025964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575076-C-T

3026088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575185-T-C

3026162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575250-G-C

3026200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575292-A-T

3026385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575460-T-C

3026433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575506-C-T

3027121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575698-T-C

3027121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575698-T-G

3027312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575865-T-C

3027357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27575910-T-G

3027633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576170-G-T

3027696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576221-G-A

3027696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576221-G-C

3027876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576389-A-G

3027885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576398-T-C

3027893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576405-T-C

3028156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27576671-G-A

3028530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577007-G-A

3028530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577007-G-C

3029111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577611-G-A

3029155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577652-A-G

3029244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577729-C-T

3029258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577743-T-C

3029355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577835-T-C

3029380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27577860-G-A

3030602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579645-T-C

3030774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579817-C-T

http://identifiers.org/hco/9/GRCh38#3030818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27579861-C-A

3030970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27579985-A-G

3031196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580198-C-T

3031278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580274-G-A

3031312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580313-A-G

http://identifiers.org/hco/9/GRCh38#3031322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27580323-A-C

3031414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580583-T-C

3031676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580854-G-A

3031676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27580854-G-C

3032072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581249-T-C

3032397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581472-C-T

3032534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581611-G-C

3032552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581629-T-C

3032635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581694-G-A

3032649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581708-C-T

3032749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581809-G-A

3032749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27581809-G-C

3033270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582315-T-A

3033274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582319-A-T

http://identifiers.org/hco/9/GRCh38#3033310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27582350-C-A

3033358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582398-G-T

http://identifiers.org/hco/9/GRCh38#3033366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27582406-A-C

3033401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582441-G-A

3033451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582468-C-T

3033503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582519-C-T

http://identifiers.org/hco/9/GRCh38#3033672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27582735-A-C

3033829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27582944-A-T

3033905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583049-G-A

3033905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583049-G-T

3033921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583065-T-C

3034095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583222-C-G

3034140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583272-C-G

3034140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583272-C-T

3034184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583320-A-G

3034217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583351-G-A

3034303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583700-T-G

3034531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27583969-C-T

3034596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584032-G-T

3034638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584073-T-C

3034871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584333-T-C

3035044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584523-G-A

3035164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27584642-A-G

3035423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585551-A-G

3035459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585587-G-T

3035496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585624-G-A

3035496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585624-G-C

3035587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585719-T-A

3035653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585786-C-G

3035668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585801-G-C

3035673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585806-G-A

3035673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585806-G-C

http://identifiers.org/hco/9/GRCh38#3035677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27585810-C-A

3035677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585810-C-G

3035701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585834-T-C

3035773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585909-G-A

3035847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27585969-G-A

3035964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586070-G-T

http://identifiers.org/hco/9/GRCh38#3036071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27586181-C-A

3036107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586213-T-C

http://identifiers.org/hco/9/GRCh38#3036108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27586214-C-A

3036108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586214-C-T

3036155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586263-G-A

3036388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586500-C-G

3036389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586501-T-C

3036390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586502-G-C

http://identifiers.org/hco/9/GRCh38#3036482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27586601-C-A

3036554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586671-C-T

3036558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586675-T-G

3036567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586682-T-C

3036598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586713-A-G

3036603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586717-C-T

3036659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586763-T-C

3036675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586779-A-G

http://identifiers.org/hco/9/GRCh38#3036678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27586787-A-C

3036731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586841-C-T

3036758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586868-C-G

3036889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27586972-A-T

http://identifiers.org/hco/9/GRCh38#3037016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27587093-A-C

3037086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587156-C-T

3037147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587215-A-G

3037248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587574-G-A

3037335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27587656-G-A

3038267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27589259-A-G

3038267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27589259-A-T

3038340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27589333-G-C

3038356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27589349-A-G

http://identifiers.org/hco/9/GRCh38#3040296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27590470-C-A

3040297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590471-A-G

3040401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590558-A-G

3040415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590567-G-A

3040485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590626-A-T

http://identifiers.org/hco/9/GRCh38#3040524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27590665-C-A

3040524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590665-C-T

3040525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590666-T-C

3040570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590710-G-T

3040584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590724-G-A

http://identifiers.org/hco/9/GRCh38#3040621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27590733-C-A

3040625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590737-C-T

3040806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590902-A-G

3040840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590964-C-T

3040853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27590977-T-A

3040945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591087-C-G

3040961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591103-G-A

3041058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591288-T-A

3041081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591311-G-T

3041141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591341-C-T

3041244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591454-T-C

3041320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591520-G-A

3041381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591583-G-T

3041492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591674-A-G

3041728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591879-A-G

3041750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27591914-T-C

3041876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592032-T-A

3041892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592048-A-G

3042024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592399-C-T

3042058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592433-T-C

3042139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592518-T-C

3042392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592706-T-G

3042442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27592754-A-T

3042745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593062-G-C

3042900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593215-G-A

3042906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593221-G-C

http://identifiers.org/hco/9/GRCh38#3042912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27593234-C-A

3042922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593244-C-T

3043143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593390-T-A

3043148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593395-G-A

3043175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593411-G-A

3043175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593411-G-C

3043200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593432-T-G

3043257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593466-A-G

3043302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593515-G-A

3043611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593759-T-A

3043611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593759-T-C

3043642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593784-C-G

3043642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593784-C-T

3043704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593846-T-C

3043769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593907-A-T

3043819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593956-G-A

3043819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27593956-G-C

3043987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594119-G-C

3044023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594136-A-G

3044044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594156-C-T

3044046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594158-T-A

3045004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594721-A-T

3045207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594966-G-C

3045211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27594970-A-G

http://identifiers.org/hco/9/GRCh38#3045677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27595431-C-A

3045695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595449-T-C

3045700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595454-T-C

3045708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595463-C-T

3045761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595552-A-G

3046058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595821-A-G

3046082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595845-C-G

3046082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595845-C-T

3046097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595853-A-G

3046148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27595903-G-C

3047606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599530-C-T

3047721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599634-G-A

http://identifiers.org/hco/9/GRCh38#3047835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27599744-C-A

http://identifiers.org/hco/9/GRCh38#3047879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27599787-A-C

3047925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599832-G-A

http://identifiers.org/hco/9/GRCh38#3047935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#27599842-C-A

3047935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599842-C-T

3048096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27599997-G-A

3048125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600026-A-G

3048195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600062-G-A

3048195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600062-G-C

3048428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600427-T-C

3048440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600439-T-C

3048445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600443-G-T

3048449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600447-T-C

3048461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600459-T-C

3048461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600459-T-G

3048508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600514-T-A

3048711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23392
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27600702-G-A