83859656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904083-G-A

83859656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904083-G-C

83859656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904083-G-T

http://identifiers.org/hco/6/GRCh38#83859698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86904125-C-A

83859698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86904125-C-G

83859698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86904125-C-T

http://identifiers.org/hco/6/GRCh38#83859751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#86904201-C-A

83859751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904201-C-T

83859809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 86904258-C-T

83859833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 86904282-T-A

83859873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904321-C-T

83859877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904325-A-G

83860017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86904381-A-G

83860298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86904487-C-T

83860708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86904863-T-C

83860916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86905092-G-T

83861224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86905367-G-A

83861224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86905367-G-C

83861224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86905367-G-T

83862406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86906494-G-C

http://identifiers.org/hco/6/GRCh38#83862596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86906629-A-C

83862596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86906629-A-G

http://identifiers.org/hco/6/GRCh38#83862717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86906717-C-A

83862900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86906893-G-C

83863132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86907445-T-C

83864309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86909134-T-C

83864334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86909159-T-A

http://identifiers.org/hco/6/GRCh38#83864450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86909222-C-A

83864450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86909222-C-T

83864481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86909253-G-C

83885394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86910711-A-G

83885506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86910821-G-A

83885617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86910948-A-G

83885646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86910973-G-T

83885660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86910987-G-A

83885662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86910989-A-G

83892957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911063-G-A

83893383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911427-G-C

83893383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911427-G-T

83893424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911462-G-T

83893442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911478-T-G

83893444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911480-T-G

83893535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86911570-T-C

83893541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86911576-C-G

83893638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911671-A-G

83893752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911772-G-A

83893752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86911772-G-T

83894055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86912073-A-G

http://identifiers.org/hco/6/GRCh38#83894390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86912428-C-A

http://identifiers.org/hco/6/GRCh38#83908711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86914207-C-A

83908713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914209-G-A

83908731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914231-T-G

83908882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914333-A-T

83908918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914348-G-A

83908928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914358-G-A

83909093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914517-A-G

http://identifiers.org/hco/6/GRCh38#83909177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86914576-A-C

83909177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914576-A-G

http://identifiers.org/hco/6/GRCh38#83909201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86914599-C-A

83909213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914610-G-A

83909213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86914610-G-T

83912628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86918654-T-A

83912650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86918676-A-G

83913262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86919247-T-C

83913290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86919274-A-G

83913328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86919313-A-G

83913331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86919316-T-C

83913371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86919356-G-A

83913603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86919552-G-A

83914049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920040-T-C

83914325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920364-G-A

83914325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920364-G-C

83914325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920364-G-T

83914369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920736-A-G

83914489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920852-G-A

83914489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920852-G-T

83914524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920887-G-A

83914524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920887-G-T

83914856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920905-T-A

83914913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86920961-G-C

83915194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921166-T-C

83915343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921318-T-A

83915391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921353-A-G

83915434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921390-A-G

83915449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921405-G-A

83915502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921457-A-G

83915602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921507-A-G

83915700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921595-G-C

83915716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921619-T-C

83915994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86921916-C-T

83917922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922371-G-A

83917922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922371-G-T

83918050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86922504-G-A

83918050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86922504-G-T

83918079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922534-T-C

83918118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922568-G-A

83918118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922568-G-C

http://identifiers.org/hco/6/GRCh38#83918123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86922573-C-A

83918123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922573-C-G

83918123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922573-C-T

83918141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922587-G-T

83918448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86922865-T-G

83918619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923033-T-A

83918670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923082-T-G

http://identifiers.org/hco/6/GRCh38#83919373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86923280-C-A

83919373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923280-C-T

83919432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86923341-T-C

83919492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923392-T-C

83919494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923394-A-G

83919496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923396-T-A

83919496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923396-T-C

83919506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923408-T-C

83919515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923417-T-C

83919558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923448-A-G

83920001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86923874-A-G

83920221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924003-C-T

83920758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924521-T-G

83920952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924716-A-G

83920980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924742-A-G

83920981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924743-A-G

83921094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86924845-G-A

83921094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86924845-G-T

83921106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86924857-G-A

83921106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86924857-G-T

83921142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86924893-A-G

83921156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86924907-T-C

http://identifiers.org/hco/6/GRCh38#83921183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86924934-C-A

83921189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924940-T-A

83921189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924940-T-C

http://identifiers.org/hco/6/GRCh38#83921217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86924966-C-A

83921217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924966-C-T

83921226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924975-T-C

83921249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86924998-T-G

83921446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86925211-G-A

83921967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929114-C-T

83922053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929201-C-T

83922181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929300-C-T

83922182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929301-G-A

83922198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929317-T-C

83922347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929434-G-A

83922395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929476-G-A

83922395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929476-G-T

83922540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86929654-A-G

http://identifiers.org/hco/6/GRCh38#83923074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86930429-A-C

83923074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86930429-A-T

83923755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86930782-C-G

83924120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86930860-A-T

83924256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86930953-G-C

83924256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86930953-G-T

83924291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86930988-A-G

83924308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86931005-T-G

83924396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86931082-G-T

83924476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86931161-T-A

83924495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86931180-A-G

83924578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86931263-C-G

83928790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86931993-T-C

83928816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86932019-C-T

83928831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86932034-G-C

http://identifiers.org/hco/6/GRCh38#83929185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86932435-A-C

83929255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86932501-A-G

83929562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86932753-G-T

83932185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86935582-T-G

83932196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86935593-C-T

83932348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86935736-T-C

83932431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86935796-A-G

83932437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86935802-T-G

83932531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86935847-G-A

83932779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936100-G-A

83932897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936206-C-G

83932941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936244-G-T

83932996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936287-T-C

83933160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936666-A-G

83933230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936737-G-A

83933293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936767-T-C

83933305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936772-A-G

83933306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936773-T-C

83933331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936803-G-A

http://identifiers.org/hco/6/GRCh38#83933334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86936807-A-C

83933334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936807-A-T

83933446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936918-G-A

83933459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86936931-T-G

83933610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937077-A-G

83933625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937093-C-T

83933754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937196-T-C

83933880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937291-A-T

83933997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937383-G-A

http://identifiers.org/hco/6/GRCh38#83934221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86937542-C-A

83934221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937542-C-G

83934278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937590-C-T

83934516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937780-G-C

83934516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937780-G-T

83934535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86937799-G-A

83934657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86937880-T-C

83934710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86937933-T-C

83934933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938088-A-T

83934938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938093-A-G

83935017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938112-G-C

83935049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938134-G-A

83935086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938164-G-A

http://identifiers.org/hco/6/GRCh38#83935122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86938201-A-C

83935122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938201-A-G

83935288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938373-G-A

83935599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938640-G-A

83935599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938640-G-C

83935794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938812-C-T

83935998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86938984-G-T

83936082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86939051-T-C

83936082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86939051-T-G

83936122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86939097-T-C

83936314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86939285-A-G

83936391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86939362-A-G

83936436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86939402-C-G

83936560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86939499-G-A

http://identifiers.org/hco/6/GRCh38#83936983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86939927-C-A

83939209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940407-T-C

83939306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940506-T-C

83939478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940611-C-T

83939591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940726-A-G

83939927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940877-A-T

83939952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940901-T-A

83939952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940901-T-G

83939953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940902-G-A

http://identifiers.org/hco/6/GRCh38#83939992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86940922-C-A

83939992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940922-C-T

83940007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940937-T-C

83940007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940937-T-G

83940008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940938-G-A

83940008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940938-G-T

83940012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940942-T-C

83940012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86940942-T-G

http://identifiers.org/hco/6/GRCh38#83940087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86941009-C-A

83940087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86941009-C-T

83940130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86941052-T-A

83940130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86941052-T-C

83940135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86941057-G-A

83940218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941140-T-G

83940258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941175-A-G

83940346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941258-T-G

83940424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941320-A-T

83940459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941355-T-C

83940551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86941454-T-A

83940551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86941454-T-C

http://identifiers.org/hco/6/GRCh38#83940572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86941475-A-C

83940572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86941475-A-G

83940984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941578-T-C

83940989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941583-G-A

83940989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941583-G-C

83941396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86941883-A-G

83941584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86942055-A-G

83941689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86942148-C-T

83952068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86946846-T-A

83952132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86946878-G-A

83952217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86946922-T-C

83955088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86948502-T-C

83955213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86948620-G-T

83955451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86948855-A-G

83955451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86948855-A-T

83955497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86948890-A-G

83955497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86948890-A-T

http://identifiers.org/hco/6/GRCh38#83955675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86949058-C-A

83955675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949058-C-T

83955752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949120-G-A

http://identifiers.org/hco/6/GRCh38#83955767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86949135-C-A

83955767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949135-C-T

83955899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949270-G-A

http://identifiers.org/hco/6/GRCh38#83955924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86949300-A-C

83956004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949346-G-A

83957759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949952-A-G

83957787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86949979-G-C

83957867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86950055-A-T

83959039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86957966-G-A

83959346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958223-C-T

83959465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958528-C-T

83959511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958586-C-G

83959533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958606-T-C

83959721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958789-G-A

83959721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958789-G-T

83959754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958814-T-C

83959762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958824-T-C

http://identifiers.org/hco/6/GRCh38#83959773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#86958835-C-A

83959773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958835-C-T

83959815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86958872-G-T

83959842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86958899-C-G

83959965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959016-A-G

83960071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959103-A-G

83960083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959114-C-G

83960083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959114-C-T

83960201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959232-A-G

83960201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959232-A-T

83960224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959255-C-G

83960224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959255-C-T

83960610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959893-A-G

83960655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86959934-A-G

83960849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86960056-T-A

83960854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86960061-C-T

83961129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86960246-G-A

83961137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86960254-T-C

83961303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20147
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86960363-A-G