87503373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916764-T-C

87503513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916636-T-C

http://identifiers.org/hco/7/GRCh38#87503566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8916583-A-C

87503567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916582-T-C

87503572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916577-C-T

87503637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916525-G-C

87503647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916515-A-G

87503685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916479-G-T

87503746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916418-A-G

http://identifiers.org/hco/7/GRCh38#87503806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8916362-C-A

87503858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916313-T-A

87503858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916313-T-C

87503859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3 prime UTR variant
orthologous variants: 8916312-C-T

87503985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916203-T-G

87504030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916161-T-G

87504035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916156-A-T

87504046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916129-A-T

87504054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916121-T-C

87504054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916121-T-G

87504071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916100-T-C

87504096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916074-A-G

87504173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8916019-T-C

87504319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8915878-G-A

87504319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8915878-G-C

87504319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8915878-G-T

87504322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8915875-C-T

87504920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8797195-G-T

87505366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8914665-T-G

87505502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8914549-A-G

87505745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8914373-G-T

87505811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8914307-G-A

87505811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8914307-G-T

87505889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8914267-A-G

87505967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8914189-G-A

87506065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8914091-T-C

87506065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8914091-T-G

87506067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8914089-T-A

87506067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8914089-T-C

87506067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8914089-T-G

87506078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8914078-C-T

87506235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8913934-T-C

87506747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8913454-C-T

http://identifiers.org/hco/7/GRCh38#87507261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8791779-C-A

87507261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8791779-C-T

87507644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8912575-C-T

87507703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8912513-G-A

87507703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8912513-G-T

87508645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8912116-C-T

http://identifiers.org/hco/7/GRCh38#87508694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8912067-A-C

87508694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8912067-A-G

87508851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911930-C-T

87508873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911916-A-G

87508880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911909-T-A

87508880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911909-T-C

87509037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911795-T-C

87509140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911698-G-T

87509363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8911540-C-T

87509423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8911480-C-T

87509599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911306-T-C

87509606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8911299-T-C

87510074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910792-A-G

87510267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910538-A-G

87510318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910472-T-C

87510362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910439-T-C

87510372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910429-G-A

87510603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910252-G-A

87510756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910127-C-G

87510756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8910127-C-T

87510918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909812-T-C

87510963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909759-T-C

http://identifiers.org/hco/7/GRCh38#87511082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8909673-A-C

87511121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909628-G-A

87511196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909555-C-G

87511262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909492-T-C

87511268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909486-T-C

87511299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909455-A-G

87511404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909353-T-C

87511405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909352-A-G

87511458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909306-T-C

87511558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909212-A-T

87511594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8909179-T-A

87512154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8908862-A-T

87514330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789815-G-A

87514509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789552-T-C

87514528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789536-A-G

87514561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8789503-C-T

87514809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8903947-G-A

87514841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8903918-T-C

87514919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8903835-C-T

87515148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8903691-A-G

87515316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8903539-A-T

87515471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8903384-T-C

87515477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8903378-T-C

87516479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8901641-T-C

http://identifiers.org/hco/7/GRCh38#87516618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8901502-C-A

http://identifiers.org/hco/7/GRCh38#87516708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8901412-A-C

87516708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8901412-A-G

87516851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8901242-C-T

87517239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8900688-G-A

http://identifiers.org/hco/7/GRCh38#87517320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8900616-C-A

87517320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8900616-C-T

87517432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8900514-C-T

87517445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8900501-G-C

87518088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8900024-T-G

87518141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8899946-T-C

87518611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786717-T-C

87518627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786701-A-G

87518809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8786519-T-G

87519358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8783705-T-A

87519479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783584-C-T

87519491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783573-C-T

87519528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783544-T-C

87519556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783516-G-A

87519556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783516-G-T

87519572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783501-T-G

http://identifiers.org/hco/7/GRCh38#87519579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8783494-C-A

87519579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783494-C-T

87519633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783443-T-C

87519808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783289-G-A

87519926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783190-G-C

87519953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8783164-T-G

http://identifiers.org/hco/7/GRCh38#87520248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8782891-C-A

87520407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8782733-C-T

87520554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8782592-A-G

http://identifiers.org/hco/7/GRCh38#87520630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8782519-C-A

http://identifiers.org/hco/7/GRCh38#87520675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8782487-C-A

87520746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8782420-A-G

87520923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782249-G-A

87520923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782249-G-T

87520929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782243-T-C

87520989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782176-A-G

87521018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782147-A-G

87521018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782147-A-T

87521102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8782078-A-G

87521136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8782048-A-G

http://identifiers.org/hco/7/GRCh38#87521183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8895470-C-A

87521189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8895464-T-C

87521190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8895463-T-A

87521190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8895463-T-G

87521191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8895462-G-A

87521191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8895462-G-T

87521235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8895414-T-C

87523052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8781238-A-G

87523683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780504-C-T

87523730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780459-G-A

87523826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780370-C-T

87523936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780292-T-A

87523985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780236-C-T

87524143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780073-T-C

87524158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8780054-G-A

87524399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8779884-G-A

87524487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8779800-A-G

87524759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8779553-G-T

87524851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8779437-G-C

87524900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8779373-T-C

87525263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8889578-G-T

http://identifiers.org/hco/7/GRCh38#87525375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8889462-C-A

87530693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8778296-C-T

87530801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8778189-G-A

87530805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8778185-G-A

87530821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8778169-G-T

87530949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8888093-G-A

87531170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8887950-A-G

87531203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8777058-A-T

87531213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8777048-A-G

87531251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8777014-C-G

87531284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8776984-T-C

87531537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8776735-A-G

87531537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8776735-A-T

87531643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8776643-T-C

87531992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8776360-G-A

87532030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8776329-T-G

http://identifiers.org/hco/7/GRCh38#87532073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8776286-A-C

87533206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8775658-C-T

87533253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8775621-A-G

87533469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8775462-T-C

http://identifiers.org/hco/7/GRCh38#87534938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8775102-A-C

87535159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774902-C-T

87535656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774383-T-C

http://identifiers.org/hco/7/GRCh38#87535710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8774334-C-A

87535710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774334-C-G

87535711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774333-A-G

87535820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774234-T-C

87535820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774234-T-G

87535821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774233-T-A

87535870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8774182-G-A

87536351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8773345-A-G

87536504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8773194-C-T

http://identifiers.org/hco/7/GRCh38#87536641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8773058-C-A

87536641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8773058-C-G

87536643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8773056-T-C

87536777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8772953-G-A

http://identifiers.org/hco/7/GRCh38#87537004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8772680-C-A

87537004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8772680-C-G

http://identifiers.org/hco/7/GRCh38#87537048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8772639-C-A

87537048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8772639-C-T

http://identifiers.org/hco/7/GRCh38#87537168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8772571-C-A

87537168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8772571-C-T

87537263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8772508-T-A

87537263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8772508-T-C

87537711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8772175-T-C

http://identifiers.org/hco/7/GRCh38#87537712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8772174-C-A

87537786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8772109-C-G

87538120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8771143-C-G

87538335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8770791-T-C

87539091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8770213-C-G

87539091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8770213-C-T

http://identifiers.org/hco/7/GRCh38#87539103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8770201-A-C

87539170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8770165-T-G

87539210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8770123-C-T

87539214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8770119-G-A

http://identifiers.org/hco/7/GRCh38#87539284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8770050-C-A

87539284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8770050-C-T

87539553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769912-T-C

87539987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769597-T-C

87540000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769584-A-T

87540741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8879504-C-T

87540753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8879491-A-G

87540765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8879479-T-C

87540816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8879428-G-A

http://identifiers.org/hco/7/GRCh38#87540868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8879369-A-C

87540881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8879356-A-G

87541003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769398-A-G

87541054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769347-A-G

87541189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769206-A-G

http://identifiers.org/hco/7/GRCh38#87541232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8769185-C-A

87541232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769185-C-G

87541232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769185-C-T

87541287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769129-T-A

87541287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769129-T-C

87541303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769113-G-A

87541303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8769113-G-T

87541393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: synonymous variant
orthologous variants: 8769048-G-T

87541444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: synonymous variant
orthologous variants: 8768997-A-G

87541444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8768997-A-T

87541547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8768900-T-C

http://identifiers.org/hco/7/GRCh38#87541604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8768839-C-A

87541692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8878638-G-A

http://identifiers.org/hco/7/GRCh38#87541781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8878551-C-A

87541934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8768081-C-T

87542078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8767939-C-G

87542309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8767747-A-G

http://identifiers.org/hco/7/GRCh38#87542566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8767526-C-A

87543740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8766336-G-A

87543882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8766196-C-G

87543882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8766196-C-T

87544018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8766050-A-T

87544026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8766042-G-A

87544088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765927-A-T

87544109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765907-C-G

87544109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765907-C-T

http://identifiers.org/hco/7/GRCh38#87544594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8765307-A-C

87544685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765219-A-G

87544686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765218-A-G

87544687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765217-T-C

87544687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765217-T-G

http://identifiers.org/hco/7/GRCh38#87544728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8765158-C-A

87544728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765158-C-T

87544742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765143-A-G

87544742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765143-A-T

87544788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765094-T-C

87544788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8765094-T-G

87545082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8764817-G-A

87545082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8764817-G-T

87545113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8764788-A-T

http://identifiers.org/hco/7/GRCh38#87545815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8763394-C-A

87546155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8763063-G-T

87546678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8762838-A-G

87546691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8762825-A-G

http://identifiers.org/hco/7/GRCh38#87546862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8762690-C-A

87547155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8762387-C-T

87547236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754390-T-C

87547315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754295-A-G

87547317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754293-G-C

87547317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754293-G-T

87547332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754278-C-T

87548437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754117-A-G

87548504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754056-T-C

87548519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8754047-T-G

87548814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8753790-T-C

87548964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753558-T-G

87549064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753460-G-C

87549293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8753015-A-G

87549427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752882-G-A

87549442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752867-G-A

87549446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752863-G-A

87549446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752863-G-T

87549580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752765-A-G

87549584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752761-G-T

87549702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752716-T-C

87549723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752695-A-G

http://identifiers.org/hco/7/GRCh38#87549752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8752671-C-A

87549766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752657-T-C

87549815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8752604-G-C

87549999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752422-A-G

87550038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752383-T-C

87550041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8752380-C-T

87550077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8752348-C-T

87550102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8752326-G-C

87550124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8752308-T-A

87550124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8752308-T-C

87550196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8752251-C-G

87550250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8752197-G-A

87550262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8752185-C-T

87550357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8752088-G-C

87550707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8751737-T-C

87550709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8751735-G-A

87550709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8751735-G-T

87550735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8751710-A-T

87550771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8751674-G-A

87550771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8751674-G-T

87550861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8751584-A-G

87550967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8751483-G-A

87552131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8750899-G-T

87552303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8750756-A-G

87552444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8750642-A-G

http://identifiers.org/hco/7/GRCh38#87552507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8750579-C-A

87552732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8750270-G-A

87552732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8750270-G-T

87552801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8750201-T-C

87553668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748739-G-A

87553668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748739-G-C

87553668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748739-G-T

87553734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748688-G-T

87553989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748420-G-A

87553989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748420-G-C

http://identifiers.org/hco/7/GRCh38#87554002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8748407-A-C

87554008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748401-G-T

87554034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748375-T-A

87554034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748375-T-C

http://identifiers.org/hco/7/GRCh38#87554071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8748346-A-C

87554071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748346-A-G

87554097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748319-T-C

87554144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8748274-G-A

87554290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8747953-C-T

87554600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8747693-C-T

87554883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8747183-G-A

87554951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8747097-G-C

http://identifiers.org/hco/7/GRCh38#87555006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8747040-C-A

87555033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8747016-T-C

87555077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8746983-G-A

87555085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8746975-C-G

87555085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8746975-C-T

87555280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8746659-C-T

87555862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8746145-A-G

87556204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8745756-T-C

87556859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8745044-C-T

87556886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8745017-G-A

87556938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8744964-G-T

87557008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8744895-T-G

http://identifiers.org/hco/7/GRCh38#87561059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8744365-A-C

http://identifiers.org/hco/7/GRCh38#87561112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8744320-C-A

87561112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8744320-C-T

87561462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8744008-T-C

87561487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8743985-T-C

87562695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8742532-A-G

87562751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8742477-T-A

87564793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8737924-T-C

87564793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8737924-T-G

87565143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8737598-T-C

http://identifiers.org/hco/7/GRCh38#87565150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8737591-A-C

87565407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8737361-A-T

87565656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8737061-T-C

http://identifiers.org/hco/7/GRCh38#87565999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8736353-A-C

http://identifiers.org/hco/7/GRCh38#87566005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8736347-C-A

http://identifiers.org/hco/7/GRCh38#87566307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8736048-C-A

87566345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8736003-T-A

87566349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735997-C-T

87566361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735983-T-G

87566374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735970-G-A

87566374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735970-G-C

87566374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735970-G-T

87566477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735872-A-G

87566515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735834-G-A

87566515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735834-G-C

87566523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735824-C-T

87566527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735820-T-G

http://identifiers.org/hco/7/GRCh38#87566558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8735716-C-A

87566605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735580-C-T

87566657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735533-G-A

87566657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735533-G-T

87566711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735490-G-A

http://identifiers.org/hco/7/GRCh38#87566821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8735374-A-C

87566821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant
orthologous variants: 8735374-A-G

87566910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 8735285-A-G

87566917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant
orthologous variants: 8735278-A-G

87566959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant
orthologous variants: 8735236-C-G

87566959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant
orthologous variants: 8735236-C-T

87566974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 8735221-T-A

87566974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 8735221-T-C

87567073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735133-G-A

87567073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735133-G-T

87567138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735072-C-T

87567207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8735019-C-T

87567291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734945-C-G

87567291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734945-C-T

87567327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734909-T-C

http://identifiers.org/hco/7/GRCh38#87567444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8734795-A-C

87567476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734763-T-A

87567518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734721-A-G

http://identifiers.org/hco/7/GRCh38#87567628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8862139-C-A

87567680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8862086-T-C

87568627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734336-A-G

87568641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734330-C-G

87568766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734210-T-A

87568797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8734197-G-A

87569100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8861341-A-T

87569415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733950-T-G

87569425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733940-C-T

87569473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733896-G-A

87569473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733896-G-T

87569512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733853-T-A

87569598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733791-G-C

http://identifiers.org/hco/7/GRCh38#87570116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8733493-C-A

http://identifiers.org/hco/7/GRCh38#87570213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8733392-A-C

87570213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: synonymous variant
orthologous variants: 8733392-A-G

http://identifiers.org/hco/7/GRCh38#87570248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8733355-C-A

87570248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733355-C-G

87570281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733322-A-G

87570415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8733201-T-C

87570725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8732745-T-G

87570728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8732742-A-G

87570848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8732550-A-G

87571181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8732260-T-C

87571200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8732241-G-A

87571521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8731932-T-C

87571529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8731924-A-G

87571564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8731889-G-C

87571735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8731731-A-T

87571842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8731592-T-C

http://identifiers.org/hco/7/GRCh38#87573523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8731117-C-A

87573627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8731014-C-T

87573993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8730672-C-T

87574152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8730523-T-C

87574436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8730149-T-C

http://identifiers.org/hco/7/GRCh38#87574529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8730060-C-A

87574785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8729777-C-G

87574871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8729690-T-C

87575016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8729550-A-T

87575088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8729484-T-C

87581320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8859294-C-T

87581389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8859229-C-T

http://identifiers.org/hco/7/GRCh38#87584530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8725951-C-A

http://identifiers.org/hco/7/GRCh38#87584941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8856745-A-C

87585051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8725280-G-C

http://identifiers.org/hco/7/GRCh38#87585085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8725243-C-A

87585085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8725243-C-T

87585167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8725166-C-T

87585182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8725150-T-C

87585302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8725030-T-C

87585406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724946-G-A

87585406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724946-G-T

87585448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724905-A-G

87585448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724905-A-T

http://identifiers.org/hco/7/GRCh38#87585483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8724870-A-C

87585483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724870-A-G

http://identifiers.org/hco/7/GRCh38#87585511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: splice donor variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8724841-C-A

87585521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: missense variant
orthologous variants: 8724831-T-C

87585766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724612-T-C

87585864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724488-G-T

87585983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8724377-A-G

87586449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8723832-G-A

http://identifiers.org/hco/7/GRCh38#87586520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8723727-C-A

87586520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8723727-C-T

87587003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8723259-T-A

87587125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8723143-T-C

87587507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8722736-A-G

http://identifiers.org/hco/7/GRCh38#87589138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8721178-A-C

87590008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8720234-G-C

87590259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8720018-A-G

87590491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719808-G-T

87590492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719807-G-A

87590492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719807-G-C

87590606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719709-A-G

87590697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719636-T-G

87590813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719496-A-G

87590890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719421-G-A

87590940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719389-T-C

87590998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719329-T-G

87591171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8719182-G-A

87591414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718922-G-C

87591417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718918-G-T

87591570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718788-A-G

87591874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718560-G-A

87591901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718536-G-A

87591950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718492-G-A

87592022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718431-A-G

87592317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718101-A-G

87592317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8718101-A-T

87592479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8717940-G-A

87592513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8717906-T-A

87592842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8717603-A-G

87593371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8717382-G-A

87593371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8717382-G-T

87593879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8716948-T-C

http://identifiers.org/hco/7/GRCh38#87593959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8716777-A-C

http://identifiers.org/hco/7/GRCh38#87594026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8716713-A-C

87594095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8716637-T-C

87594219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8716280-G-T

87594422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8716028-G-A

87594656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8715545-G-C

87594832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8715348-A-G

87595466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714884-T-C

87595471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714879-T-C

87595579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714768-T-A

87595662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714688-A-T

87595688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714657-G-T

87595700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714645-C-G

http://identifiers.org/hco/7/GRCh38#87595833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8714524-A-C

87595833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714524-A-T

87595854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714499-T-C

87595900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8714452-T-C

87596301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8713595-G-A

http://identifiers.org/hco/7/GRCh38#87596469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8713442-C-A

87596546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8713369-G-A

87596585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8713330-A-G

87596693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8713239-T-C

87596772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8712951-T-C

87596892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8712833-A-G

87597205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8712532-A-G

87597537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8712130-A-G

87597743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8711850-A-G

87598168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8850378-T-C

87598212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8850346-T-C

http://identifiers.org/hco/7/GRCh38#87598228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8850340-A-C

87598592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8849990-G-A

87598592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8849990-G-T

87598680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8849832-T-C

87598813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8849632-G-A

87598830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8849615-C-T

87599135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8849344-T-C

87599513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8849011-C-T

http://identifiers.org/hco/7/GRCh38#87599991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8710851-C-A

87600073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710774-A-G

87600086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710761-G-A

87600222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8710628-G-A

87600222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8710628-G-T

87600244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8710617-A-T

87600340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710529-T-C

http://identifiers.org/hco/7/GRCh38#87600352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8710517-C-A

87600356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710513-T-G

87600368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710501-C-G

87600391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710491-T-A

87600515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710385-G-C

87600586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710327-G-A

87600662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710276-A-G

87600686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron variant
orthologous variants: 8710263-T-G

87600698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8710251-G-C

87600698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, undefined
orthologous variants: 8710251-G-T

http://identifiers.org/hco/7/GRCh38#87600774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8710183-C-A

87600774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 8710183-C-T

87600867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8710109-A-G

87601057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8709913-T-C

87601078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 8709898-T-C

87601107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8709872-T-C

87601668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8702889-T-G

87601797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8702789-C-G

87602504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8846073-T-C

87602873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8845909-C-T

87602992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8845824-T-C

http://identifiers.org/hco/7/GRCh38#87603039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8845774-C-A

87603039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8845774-C-T

http://identifiers.org/hco/7/GRCh38#87603050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8845763-C-A

87603050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8845763-C-T

http://identifiers.org/hco/7/GRCh38#87603119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8845695-C-A

87603145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8845669-G-A

87604530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700920-G-A

http://identifiers.org/hco/7/GRCh38#87604538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8700912-A-C

87605348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700396-G-A

87605357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700387-C-T

http://identifiers.org/hco/7/GRCh38#87605379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8700371-C-A

87605379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700371-C-G

87605463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700295-C-T

87605467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700291-A-G

87605493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700273-T-G

87605592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8700159-A-G

87605799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8699996-T-C

87605831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8699964-T-C

87608526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8699085-A-G

http://identifiers.org/hco/7/GRCh38#87608858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8698750-C-A

87609071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698539-C-G

87609127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8698483-T-G

87609499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8694466-C-T

87609507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8694450-G-A

87609977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8694093-C-T

87610031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8694038-A-T

87610169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8693927-G-A

87610169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8693927-G-C

87610169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8693927-G-T

http://identifiers.org/hco/7/GRCh38#87614627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8683614-C-A

87614627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683614-C-G

87614627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683614-C-T

87614705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683560-T-C

87614735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683530-C-T

87615915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8680191-G-A

87615915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8680191-G-C

87619253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678078-A-G

87619663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677982-A-T

87619687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677958-A-G

87619970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677741-A-G

87620090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677663-T-C

87625341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8676288-A-G

87627613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8673770-G-A

87627613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8673770-G-C

http://identifiers.org/hco/7/GRCh38#87627675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673716-C-A

87627718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8673673-G-A

http://identifiers.org/hco/7/GRCh38#87627904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673523-C-A

87627904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673523-C-T

http://identifiers.org/hco/7/GRCh38#87627906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673521-C-A

87628164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673277-C-T

87628192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673249-C-T

87628212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673233-G-A

87628312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673137-T-G

87628341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673108-G-T

http://identifiers.org/hco/7/GRCh38#87628357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673092-C-A

87628393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673050-G-A

http://identifiers.org/hco/7/GRCh38#87628402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#8673041-C-A

87628402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8673041-C-T

87628508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 8672948-G-A

http://identifiers.org/hco/7/GRCh38#87628527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672928-C-A

87628545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672898-A-T

87628552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672892-G-A

87628552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672892-G-T

87628615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672818-G-A

http://identifiers.org/hco/7/GRCh38#87628693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672741-C-A

87628693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672741-C-T

http://identifiers.org/hco/7/GRCh38#87628734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672693-C-A

87628734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672693-C-G

87628734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672693-C-T

http://identifiers.org/hco/7/GRCh38#87628819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672615-C-A

87628819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672615-C-T

87628864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672567-G-A

87628864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672567-G-T

87628899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672532-G-A

87628899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672532-G-C

87628899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672532-G-T

87629039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672452-G-A

87629168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672321-T-C

http://identifiers.org/hco/7/GRCh38#87629218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8672275-C-A

87629218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672275-C-G

87629218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8672275-C-T

87629232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672261-A-G

87629970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8671958-A-G

87632387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670720-T-G

87632441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670670-T-G

87632708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670276-G-A

87632734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8670249-G-T

87635227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8668189-T-G

87635271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8668153-A-G

87635503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8667927-C-T

87646683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8655169-T-A

87650690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8654094-G-T

87650700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8654084-A-T

http://identifiers.org/hco/7/GRCh38#87650802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8654015-C-A

87650802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8654015-C-T

http://identifiers.org/hco/7/GRCh38#87650945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8653860-C-A

87650945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8653860-C-G

87650945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 8653860-C-T

http://identifiers.org/hco/7/GRCh38#87651040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8652097-C-A

87651083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8652026-A-G

87651501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651436-G-A

87651501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651436-G-C

http://identifiers.org/hco/7/GRCh38#87651535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8651410-A-C

87651593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651353-A-G

87651762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651194-A-T

87651824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651154-T-C

87651933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8651051-T-C

87652111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8645587-T-C

87652478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8645251-G-T

87652727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644924-T-C

87652844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644806-G-A

87652844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644806-G-T

87653229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8644407-G-A

http://identifiers.org/hco/7/GRCh38#87686149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8641861-A-C

87686259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8641759-T-C

87687074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8641326-A-T

87687499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8640957-G-A

87687751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8640730-T-C

87688175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8640315-A-G

http://identifiers.org/hco/7/GRCh38#87690278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8636498-A-C

87691706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8630846-A-G

87691963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8630625-T-C

87692071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8630522-A-G

87693068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629979-C-T

87693112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629935-T-C

87693123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629924-T-C

87693308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629580-A-G

87693469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629424-A-G

87693527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629373-A-G

87700402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8629175-C-T

87700660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628742-A-G

87700661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628741-G-T

87700877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628575-T-A

87700970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628503-T-C

87700970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628503-T-G

87701010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8628473-C-T

87703037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8626459-T-G

87707535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8623430-G-A

87707555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8623410-C-T

87707691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8623253-A-G

87708105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622823-T-C

87708202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622737-A-G

http://identifiers.org/hco/7/GRCh38#87708342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8622436-A-C

87708342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622436-A-G

87708348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622402-G-C

http://identifiers.org/hco/7/GRCh38#87708381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8622374-A-C

87708708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8622080-T-C

87708943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621871-C-T

87708963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621856-T-G

87709136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621684-T-C

87709141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621679-A-G

87709197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621622-T-C

http://identifiers.org/hco/7/GRCh38#87709214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8621605-C-A

87709214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621605-C-G

87709249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621572-T-C

87709411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8621397-G-T

87709431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8621378-A-G

87709432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8621377-C-T

87709524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621291-G-A

87709524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621291-G-T

87709654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621209-T-C

87709654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621209-T-G

87709828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8621038-T-C

http://identifiers.org/hco/7/GRCh38#87709991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8620074-A-C

87709991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8620074-A-G

87710161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619906-T-C

87710337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619791-C-T

http://identifiers.org/hco/7/GRCh38#87710439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8619696-C-A

87710664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619484-G-A

87710664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619484-G-C

87710748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619425-T-C

http://identifiers.org/hco/7/GRCh38#87710755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8619418-C-A

87710782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619391-C-T

http://identifiers.org/hco/7/GRCh38#87710796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8619377-C-A

87710796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619377-C-T

87710866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619302-C-T

87710886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619282-T-C

87710886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619282-T-G

87711444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8619018-G-C

87711502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618959-G-T

87711653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618802-A-T

http://identifiers.org/hco/7/GRCh38#87711669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8618785-A-C

87711904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618598-C-T

87711955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618547-G-C

87711962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618540-T-C

87712020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618485-T-A

http://identifiers.org/hco/7/GRCh38#87712162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8618155-C-A

87712163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618154-C-T

87712246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8618079-A-G

http://identifiers.org/hco/7/GRCh38#87712901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#8617484-A-C