http://identifiers.org/hco/3/GRCh38#123585269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34842618-C-A

123585269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 34842618-C-G

123585269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 34842618-C-T

123585319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non coding transcript exon variant
orthologous variants: 34842561-C-T

123585394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 34842498-A-G

http://identifiers.org/hco/3/GRCh38#123585407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34842485-A-C

http://identifiers.org/hco/3/GRCh38#123585512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34842380-C-A

123585576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34842313-C-T

123585587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34842302-G-A

123585587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34842302-G-C

123585587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34842302-G-T

123585847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34842094-G-A

123585974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34841974-C-G

123585974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34841974-C-T

123589561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34840822-A-G

123595482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34830387-T-C

123595622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34830262-T-C

123595634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34830250-C-T

http://identifiers.org/hco/3/GRCh38#123595649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34830234-A-C

123595979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34829915-A-G

http://identifiers.org/hco/3/GRCh38#123596194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34829708-A-C

123605906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826073-T-C

123606123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825864-G-A

123606916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825263-G-A

http://identifiers.org/hco/3/GRCh38#123612548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34822553-C-A

123612548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822553-C-G

123612569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822532-G-T

123612574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822527-A-G

123612594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822507-T-C

123612613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822486-G-A

123612613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822486-G-T

123612658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822448-G-A

123612668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822438-G-T

123612673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822431-G-A

123612673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822431-G-T

123612683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822421-T-A

123612747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822358-G-A

123612747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34822358-G-T

123613266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821825-C-T

123613317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821775-A-G

123613471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821593-G-C

123613496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821566-G-T

123613551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821507-G-T

123614012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821006-G-A

123614012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34821006-G-T

123614024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820994-T-G

123614025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820993-T-C

123614025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820993-T-G

123614026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820992-G-T

123614217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820773-G-T

123614383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34820608-A-G

http://identifiers.org/hco/3/GRCh38#123614445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34820547-A-C

123615910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820374-A-G

123616005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34820212-G-A

123617154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34819630-G-A

http://identifiers.org/hco/3/GRCh38#123617360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34819451-A-C

123617537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34818336-T-C

123617568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34818303-A-G

123617624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34818249-A-G

123617650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34818223-G-A

123617788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34818086-G-A

123617914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817965-C-T

123617952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817916-G-A

123617952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817916-G-T

123617957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817911-A-T

123617962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817906-T-A

123617962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817906-T-C

123617996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817849-G-T

123618007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817838-C-G

http://identifiers.org/hco/3/GRCh38#123618112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34817730-C-A

123618112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817730-C-T

123618143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817699-G-T

123618179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817663-G-T

123618261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817583-G-A

123618399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817450-T-G

http://identifiers.org/hco/3/GRCh38#123618400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34817449-A-C

123618400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817449-A-G

123618400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817449-A-T

http://identifiers.org/hco/3/GRCh38#123618435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34817415-C-A

123618435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817415-C-T

123618547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817301-C-T

123618713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34817150-G-C

http://identifiers.org/hco/3/GRCh38#123618907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34816750-C-A

123618907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34816750-C-T

123619003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34816653-C-T

123619243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34816437-G-A

http://identifiers.org/hco/3/GRCh38#123620067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34815664-C-A

123620156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34815616-G-T

http://identifiers.org/hco/3/GRCh38#123620159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34815613-C-A

123620190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34815584-G-A

http://identifiers.org/hco/3/GRCh38#123620826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34815002-C-A

123620970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814850-G-T

http://identifiers.org/hco/3/GRCh38#123621449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34814652-C-A

123621466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814635-G-A

http://identifiers.org/hco/3/GRCh38#123621812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34814383-C-A

http://identifiers.org/hco/3/GRCh38#123621854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34814356-C-A

123621854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814356-C-T

123622102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814204-G-A

123622102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814204-G-T

http://identifiers.org/hco/3/GRCh38#123622106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34814200-C-A

123622106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814200-C-T

123622154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814164-C-T

http://identifiers.org/hco/3/GRCh38#123622249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34814105-C-A

123622254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34814100-G-T

123622420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813930-G-A

123622420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813930-G-T

123622439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813901-C-T

http://identifiers.org/hco/3/GRCh38#123622459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34813883-C-A

123622459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813883-C-T

123622562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813779-A-T

123622612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813730-G-A

123623017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813313-T-G

123623028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813302-G-A

123623139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813202-A-T

http://identifiers.org/hco/3/GRCh38#123623162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34813171-C-A

123623183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34813151-G-A

123623236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812842-A-G

123623321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812760-G-T

http://identifiers.org/hco/3/GRCh38#123623643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34812431-C-A

123623651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812426-T-C

http://identifiers.org/hco/3/GRCh38#123623670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34812408-C-A

123623670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812408-C-G

123623670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812408-C-T

123623740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812336-G-A

123623823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34812249-G-A

http://identifiers.org/hco/3/GRCh38#123624732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34811695-C-A

123624759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34811669-T-C

123624945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34811487-G-A

123625113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34811358-C-T

http://identifiers.org/hco/3/GRCh38#123625114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34811357-C-A

123625155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34811336-T-C

123625265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810869-G-T

123625275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810861-C-T

123625287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810849-A-G

123625312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810825-T-C

123625350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810787-G-T

123626113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810062-A-G

123626151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810022-G-C

123626164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34810009-C-T

http://identifiers.org/hco/3/GRCh38#123626175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34809993-C-A

123626202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809969-G-A

123626752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809492-T-A

123626765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809479-A-G

123626765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809479-A-T

123627046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809156-G-T

123627071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809136-T-C

123627071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809136-T-G

http://identifiers.org/hco/3/GRCh38#123627090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34809117-C-A

123627090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34809117-C-G

123627391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808882-A-G

123627424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808856-A-G

123627529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808761-C-T

123627706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808590-C-T

123627761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808547-G-T

123628017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808297-C-T

123628130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34808194-T-C

123628388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807928-G-A

123628451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807863-C-T

123629093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807363-G-A

123629202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807241-C-T

http://identifiers.org/hco/3/GRCh38#123629281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34807124-C-A

123629323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807094-A-G

123629323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807094-A-T

http://identifiers.org/hco/3/GRCh38#123629400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34807026-C-A

123629400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34807026-C-T

123629466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34806969-C-T

123629540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34806895-T-G

123629585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34806850-T-C

123629609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 34806826-G-A

http://identifiers.org/hco/3/GRCh38#123629651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34806786-A-C

123629662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806768-G-C

123629673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806757-G-A

123629711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806712-G-A

http://identifiers.org/hco/3/GRCh38#123629724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34806704-C-A

http://identifiers.org/hco/3/GRCh38#123629752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34806677-C-A

123629760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806669-T-A

123629760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806669-T-C

123629808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806624-T-A

123629813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806619-T-A

123629813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806619-T-C

123629922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806528-T-A

123629961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806495-G-A

123629961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806495-G-C

123629961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806495-G-T

123630041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806436-C-T

123630171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806327-G-A

123630227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34806280-T-C

http://identifiers.org/hco/3/GRCh38#123630353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34806153-C-A

http://identifiers.org/hco/3/GRCh38#123630436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34806090-A-C

http://identifiers.org/hco/3/GRCh38#123630586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34805945-C-A

123630586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805945-C-T

http://identifiers.org/hco/3/GRCh38#123630724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34805811-C-A

123630724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805811-C-T

123630773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805794-G-A

123630773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805794-G-T

http://identifiers.org/hco/3/GRCh38#123630781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34805786-A-C

123630822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805746-T-C

123630951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34805658-C-T

http://identifiers.org/hco/3/GRCh38#123630961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34805648-C-A

http://identifiers.org/hco/3/GRCh38#123631051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34805556-C-A

http://identifiers.org/hco/3/GRCh38#123632506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34804760-A-C

123633503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34804344-C-T

123633748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34803458-C-G

123633796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34803409-G-A

123634164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34803216-G-A

http://identifiers.org/hco/3/GRCh38#123634188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34803192-A-C

123634306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34803096-G-T

123634538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34802989-A-T

123634718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34802865-G-A

123635113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34802663-C-T

123635129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34802648-A-G

123635236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34802564-T-A

123635255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34802547-G-T

http://identifiers.org/hco/3/GRCh38#123635724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34802165-C-A

123636008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801869-C-G

123636008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801869-C-T

123636069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801799-C-T

123636295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801579-C-T

123636302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801572-C-T

123636324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801551-G-A

123636325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801550-A-G

123636494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801425-A-T

123636512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801403-G-A

123636580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801336-C-T

123636603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801318-C-G

123636611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801310-G-A

123636611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34801310-G-T

123637094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34800911-A-G

123637192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34800359-A-G

123637192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34800359-A-T

123637234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34800329-T-C

123637414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34800180-C-G

123637646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34799998-G-C

123637814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34799887-T-C

123637815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34799886-G-A

http://identifiers.org/hco/3/GRCh38#123638301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34799489-C-A

123638669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34799086-G-A

123638669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34799086-G-T

123638838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798921-T-C

123638884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798871-G-A

123639067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798686-C-T

123639074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798679-C-G

http://identifiers.org/hco/3/GRCh38#123639103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34798650-C-A

123639103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798650-C-T

123639273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798486-T-G

http://identifiers.org/hco/3/GRCh38#123639335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34798430-C-A

123639335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798430-C-T

http://identifiers.org/hco/3/GRCh38#123639436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34798338-C-A

123639436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798338-C-T

123639472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798301-C-T

123639546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798224-G-T

123639638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798127-A-T

123639639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34798126-C-G

http://identifiers.org/hco/3/GRCh38#123639910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34797834-C-A

123639961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797771-G-A

http://identifiers.org/hco/3/GRCh38#123640070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34797682-C-A

123640072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797680-G-A

123640136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797619-A-T

123640137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797618-G-T

123640153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797602-G-A

http://identifiers.org/hco/3/GRCh38#123640193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34797561-C-A

123640193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797561-C-T

123640222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797535-A-T

123640246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797512-A-G

123640496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797261-C-T

http://identifiers.org/hco/3/GRCh38#123640583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#34797163-C-A

123640583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34797163-C-T

123640919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796851-T-G

123640929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796835-C-T

123641208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796592-C-T

123641262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796550-G-T

123641290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796525-C-T

123641394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796420-C-T

123642386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796274-G-A

123642398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796259-G-A

123642648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34796022-G-A

123643079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34795429-C-T

123643179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34795384-G-A

123643271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34795285-G-A

123643698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794921-A-G

123643717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794894-T-C

123644487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42440
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794258-T-C