130853863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31028756-A-T

130853874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31028767-C-T

130853884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31028777-G-T

130853918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31028810-T-C

130854037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31028912-G-A

130854038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31028913-G-A

http://identifiers.org/hco/7/GRCh38#130854249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31029074-C-A

130854478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029282-A-T

130865651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31030080-A-G

130865720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31030145-G-T

130865828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31030254-G-A

130865987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030402-A-G

http://identifiers.org/hco/7/GRCh38#130866532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31031815-C-A

130866666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31031942-C-T

130866682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31031958-G-T

130866916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31032173-T-G

130867044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31032277-G-T

130867123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31032336-T-C

130867168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31032378-C-T

130867822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31032421-C-T

http://identifiers.org/hco/7/GRCh38#130868193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#31032790-C-A

130868193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31032790-C-T

http://identifiers.org/hco/7/GRCh38#130868281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#31032878-C-A

130868281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31032878-C-T

130868355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31032958-C-G

130869544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037725-T-C

130869894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038044-G-A

130870132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038222-A-T

130870438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038481-G-A

130870579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038595-C-T

130870653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038653-G-A

130870777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038798-G-A

130876580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039467-C-T

http://identifiers.org/hco/7/GRCh38#130876584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31039471-A-C

130876584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039471-A-T

http://identifiers.org/hco/7/GRCh38#130876683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31039554-C-A

http://identifiers.org/hco/7/GRCh38#130876689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31039560-C-A

130876689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039560-C-T

130876713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039573-G-A

130876741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039601-A-G

http://identifiers.org/hco/7/GRCh38#130876871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31039728-C-A

130876919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31039766-T-G

http://identifiers.org/hco/7/GRCh38#130876967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31039809-C-A

130880853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042641-T-G

http://identifiers.org/hco/7/GRCh38#130880854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31042642-C-A

130880854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042642-C-G

130880855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042643-T-C

130880928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042716-T-C

130880982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042759-A-G

130881015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31041889-A-G

130881045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31041922-A-G

130881255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042079-A-T

130881459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042271-T-G

http://identifiers.org/hco/7/GRCh38#130881478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31042290-C-A

130881478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042290-C-T

http://identifiers.org/hco/7/GRCh38#130881795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31042581-C-A

130881795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042581-C-G

130881795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042581-C-T

130881855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042642-G-A

130881855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042642-G-C

http://identifiers.org/hco/7/GRCh38#130881856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31042643-C-A

130881856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042643-C-T

130881866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042654-G-T

http://identifiers.org/hco/7/GRCh38#130883818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31043030-C-A

http://identifiers.org/hco/7/GRCh38#130884261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31043151-C-A

130884321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31043218-G-T

130884331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31043228-A-G

130884546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043380-T-G

130884661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31043481-C-G

130884661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31043481-C-T

130884940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043772-A-G

130885014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043835-C-T

130885042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043865-T-C

130885340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044087-C-T

130885353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044100-T-C

130886788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045377-G-A

130886851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045432-C-G

130887370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31046019-T-C

http://identifiers.org/hco/7/GRCh38#130887371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#31046020-A-C

130887874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31046482-G-C

130887874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31046482-G-T

130890288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047225-A-G

130890305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047242-T-A

http://identifiers.org/hco/7/GRCh38#130890581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31047618-A-C

130890621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047657-C-G

130890722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047767-T-C

130890856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047888-C-G

130890864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047896-C-G

130890966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047984-T-A

130891161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048173-C-G

http://identifiers.org/hco/7/GRCh38#130891439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31048401-C-A

130891506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048465-C-T

130891607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31048567-A-G

130891744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048681-C-T

130891753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048689-T-A

130891773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31048690-A-G

130893387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049316-A-G

130893441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049383-G-A

130893441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049383-G-C

130893540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049466-G-A

130893655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049574-T-C

130893701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31049613-C-G

130893747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049665-C-G

130893749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049667-T-C

130893782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31049732-G-A

130893992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050152-C-T

130894014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31050174-C-G

130894618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31050697-C-T

130894916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051124-A-G

130894936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051144-A-T

130894997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051207-T-C

130895104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051274-T-A

130895175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051349-A-G

130895179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051353-T-C

130895663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051690-C-T

130895889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051883-C-G

130895889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051883-C-T

130895899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31051894-C-T

130895916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051911-G-A

130895949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051936-T-C

130895957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31051944-G-C

http://identifiers.org/hco/7/GRCh38#130896203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31052100-A-C

130896205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052102-G-A

130896246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052145-T-A

http://identifiers.org/hco/7/GRCh38#130896296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31052200-C-A

130896296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052200-C-T

130896597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052437-C-T

130896964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052721-T-C

130896964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31052721-T-G

http://identifiers.org/hco/7/GRCh38#130896982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31052737-A-C

130899094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054257-C-T

130899104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054267-A-G

130899189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054347-T-C

130899353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054486-C-T

130899372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054505-C-T

130899404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31054537-T-C

130899799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31054894-C-T

130899927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055027-C-T

130900031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055280-G-A

130900109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055424-G-A

130900616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31055984-C-T

http://identifiers.org/hco/7/GRCh38#130901229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31056461-C-A

130901229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056461-C-T

130901232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056464-G-A

130901351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056556-G-A

130901353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056558-T-A

http://identifiers.org/hco/7/GRCh38#130901375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31056580-A-C

130901504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056709-C-T

130901587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31056791-G-A

130901648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31056842-A-G

130901726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31056920-C-T

130901783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31056977-A-T

130901793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31056987-G-A

130901872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31057127-T-C

130901959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057201-C-G

130901959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057201-C-T

130902014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31057267-G-A

130903322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058025-C-G

http://identifiers.org/hco/7/GRCh38#130903552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31058218-C-A

http://identifiers.org/hco/7/GRCh38#130904082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31058894-C-A

130904082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31058894-C-G

http://identifiers.org/hco/7/GRCh38#130904114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#31058918-C-A

130904114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31058918-C-T

130904280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059054-T-G

130904317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059094-G-C

130904369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059144-G-A

130904369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059144-G-C

130904423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059204-T-C

http://identifiers.org/hco/7/GRCh38#130904663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31059346-A-C

130904799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059448-G-A

130904799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059448-G-T

130904818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059467-G-T

130904874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059518-C-G

130904981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31059625-G-A

130905752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059880-G-A

130905783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31059914-A-T

130905907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31060025-A-G

http://identifiers.org/hco/7/GRCh38#130906061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31060182-C-A

130906196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060457-C-T

130906303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060558-A-G

130906330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060592-G-C

130906338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31060600-G-A

130909210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061870-C-G

130909262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31061929-G-C

130910471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31063060-T-C

130910487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31063070-T-C

130910929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31063402-G-A

130911060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31063539-T-C

130911117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31063609-G-A

130911493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31063910-T-C

130912110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31064427-C-G

130912117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31064434-C-T

130912251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064575-A-G

130912578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31064870-T-G

http://identifiers.org/hco/7/GRCh38#130912685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31064972-C-A

http://identifiers.org/hco/7/GRCh38#130912834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31065132-C-A

130913015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31065299-T-C

http://identifiers.org/hco/7/GRCh38#130913426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31065707-C-A

130913426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31065707-C-T

http://identifiers.org/hco/7/GRCh38#130913431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31065720-C-A

130913562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31065848-A-G

130913705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31065991-A-G

130913879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066160-C-T

130914349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066551-C-T

130914467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066664-G-A

130914467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066664-G-C

130914479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066676-G-C

130914515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066728-G-A

130914522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31066736-A-G

130915078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31066997-G-A

130915462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067267-G-A

130915576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067374-T-C

130915602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067395-G-A

130915770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067558-T-C

130915858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067649-A-G

130915875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067666-G-A

130915875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067666-G-T

130915971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31067744-T-C

http://identifiers.org/hco/7/GRCh38#130916111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31067845-A-C

130916111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31067845-A-T

130916197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067924-A-G

http://identifiers.org/hco/7/GRCh38#130916253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31067982-C-A

130916253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31067982-C-T

130916532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31068223-G-C

130917766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31069081-T-C

130918146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31069673-T-G

130918403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31069926-T-C

http://identifiers.org/hco/7/GRCh38#130918838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31070338-A-C

130919116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070550-G-C

130919142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070571-G-A

130919190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31070615-A-G

130920548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072239-A-G

130920994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31072686-A-G

http://identifiers.org/hco/7/GRCh38#130921150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31072988-A-C

130921325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073191-G-A

130921499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073355-T-C

130921504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073359-C-T

130921517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073372-G-A

130922097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073914-G-A

130922135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31073931-A-G

130922330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074090-C-T

130922393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074153-C-T

130922409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31074188-G-A

http://identifiers.org/hco/7/GRCh38#130922804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#31074574-C-A

130923821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075479-A-G

130923940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075589-T-C

130923949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075598-A-T

130924067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075691-G-C

130924101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31075718-G-A

130924106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31075723-C-T

130924216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075805-G-A

130924216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075805-G-C

130924239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31075819-C-T

130924885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076370-G-C

130926028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076821-T-G

130926045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31076832-C-G

130927386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31077698-A-T

130927492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31077798-T-C

http://identifiers.org/hco/7/GRCh38#130927530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31077823-C-A

130927646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31077913-A-G

http://identifiers.org/hco/7/GRCh38#130927676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31077933-C-A

130927676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31077933-C-T

130927914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31078044-G-T

http://identifiers.org/hco/7/GRCh38#130928284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#31078423-C-A

130928289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31078430-G-A

130928289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31078430-G-T

130928334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31078475-G-C

130928334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31078475-G-T

130928348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31078489-T-C

130928835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078568-C-G

130928835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31078568-C-T

130929483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079108-T-A

130929591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079217-T-A

130929649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079279-G-A

130929649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31079279-G-T

130930412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31079978-A-T

130930435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 43566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31080000-T-C