199955325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57445488-G-A

199955325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57445488-G-T

199955342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57445504-G-A

199955342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57445504-G-C

199955362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 57445523-C-T

199955432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57445582-G-A

199955432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57445582-G-C

199955432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 57445582-G-T

199955457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57445607-T-C

199955511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445648-G-A

199955511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445648-G-C

199955571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445705-G-A

199955571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445705-G-C

199955571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445705-G-T

http://identifiers.org/hco/2/GRCh38#199955572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#57445706-C-A

199955572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445706-C-T

199955658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445800-G-A

199955658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445800-G-C

199955658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445800-G-T

199955660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445802-G-T

199955661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445803-A-G

199955661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445803-A-T

199955664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445806-G-A

199955664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445806-G-T

199955669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445810-G-A

199955669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445810-G-C

199955669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445810-G-T

199955678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445819-G-A

199955678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445819-G-C

http://identifiers.org/hco/2/GRCh38#199955727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#57445862-C-A

199955727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445862-C-T

http://identifiers.org/hco/2/GRCh38#199955759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#57445894-C-A

199955759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57445894-C-T

http://identifiers.org/hco/2/GRCh38#199955964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57446097-C-A

199955964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57446097-C-G

199955964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 57446097-C-T

199956030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57446163-A-T

199956034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57446167-C-T

199956224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57446357-A-G

199956337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57446468-G-T

199956339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57446470-A-G

http://identifiers.org/hco/2/GRCh38#199956342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57446473-C-A

199956342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57446473-C-T

http://identifiers.org/hco/2/GRCh38#199956350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57446481-C-A

199956350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57446481-C-G

199956350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57446481-C-T

199957653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57447342-T-G

199957671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57447360-G-T

199958854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57448650-C-T

199958917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57448720-C-T

199959215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57449010-G-A

199959215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57449010-G-T

199959257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57449060-T-A

199959485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57449267-G-T

199959739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57450867-T-A

199959739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57450867-T-G

199959809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57450937-C-T

http://identifiers.org/hco/2/GRCh38#199959993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57451120-C-A

199960105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57451412-A-T

199960187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57451501-G-C

199960302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57451618-G-A

199960421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57451732-A-G

199961540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57452184-G-A

http://identifiers.org/hco/2/GRCh38#199961647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57452278-C-A

199961647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57452278-C-T

199961726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57452349-G-T

199961976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57452591-G-A

199961976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57452591-G-T

199962009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57452625-A-G

199962055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57452666-G-A

199962055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57452666-G-T

199962064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57452675-G-T

199962298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57453019-G-T

199962472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57453151-C-G

199962632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57453301-T-C

199962646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57453315-T-C

199962646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57453315-T-G

http://identifiers.org/hco/2/GRCh38#199962656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57453324-C-A

199963075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57453859-G-T

199963219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57454181-G-A

199963415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57454481-A-G

199963467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57454585-A-G

199963546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57454653-A-G

199963861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57454949-T-A

199963861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57454949-T-C

http://identifiers.org/hco/2/GRCh38#199964025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57455105-A-C

199964025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57455105-A-G

http://identifiers.org/hco/2/GRCh38#199964074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57455154-C-A

199972136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57461576-G-A

199972374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57461842-G-A

199972404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57461864-T-A

199972510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57461962-A-G

199972511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57461963-G-C

199972683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462123-T-A

199972750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462175-A-G

199972853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462276-A-G

http://identifiers.org/hco/2/GRCh38#199972868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57462291-C-A

199973268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462517-C-T

199973295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462540-G-T

199973334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462579-C-T

199973429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462635-C-T

199973680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462793-A-T

199973822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57462944-A-G

199973853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57462965-T-A

199973974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57463085-G-A

199974219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57463308-T-C

199974256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57463338-T-A

http://identifiers.org/hco/2/GRCh38#199974402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57463448-C-A

http://identifiers.org/hco/2/GRCh38#199974418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57463463-A-C

http://identifiers.org/hco/2/GRCh38#199974458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57463525-C-A

199974468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57463535-G-A

199974468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57463535-G-T

http://identifiers.org/hco/2/GRCh38#199975240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57464186-C-A

199975462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57464394-A-G

199975551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57464483-T-C

199975612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57464595-G-A

199975612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57464595-G-C

199975632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57464634-G-A

199975711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57464707-T-G

199978388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57465423-A-T

199978527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57465677-T-G

199978927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57466044-T-C

199979060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57466166-T-G

199979530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57467619-G-T

http://identifiers.org/hco/2/GRCh38#199979657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57467733-A-C

199979714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57467782-G-T

199979746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57467803-T-C

199979880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57467935-G-C

199980048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57468095-C-T

199980102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57468149-G-C

199980545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57468560-T-C

http://identifiers.org/hco/2/GRCh38#199980760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57468795-C-A

199980760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57468795-C-T

199980871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57468907-C-G

199982300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57469125-T-C

199982300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57469125-T-G

199982959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57470184-C-T

http://identifiers.org/hco/2/GRCh38#199983220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57470419-C-A

199983220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57470419-C-G

199983686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57470779-T-C

199983892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57470938-T-C

199983892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57470938-T-G

199984187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57471190-T-C

199984912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57471877-G-A

199985055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57472018-C-G

199985524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57472314-T-A

199985618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57472380-A-G

199985634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57472396-T-C

199985742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57473766-G-A

199985753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57473777-A-T

199985852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57473877-C-T

199985855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57473880-G-C

199985939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57473936-G-T

http://identifiers.org/hco/2/GRCh38#199986253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57474311-C-A

199986253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57474311-C-T

http://identifiers.org/hco/2/GRCh38#199986285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57474339-A-C

199986529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57474657-T-C

199986739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57474864-T-G

199986783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57474905-A-G

http://identifiers.org/hco/2/GRCh38#199987300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57475370-C-A

199987300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57475370-C-G

199987300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57475370-C-T

199987518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57475500-T-C

199987813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57475795-G-C

199988333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476327-T-C

199988569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476544-A-G

199988571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476546-G-T

199988683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476664-G-A

199988688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476669-C-G

199988807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476790-G-A

199988851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476834-A-T

199988854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57476837-C-T

199989079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57477063-G-C

199989079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57477063-G-T

199989256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57477232-G-A

199989291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57477267-A-G

199990218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57479245-G-A

199990337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57479363-T-A

199992416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57481064-C-T

199992471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57481115-A-G

199992606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57481242-G-A

199992799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483400-G-A

199992799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483400-G-C

199992907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483512-G-C

199993016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483607-G-C

199993059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483651-T-C

199993225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483828-C-G

199993225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483828-C-T

199993386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57483988-T-A

199993525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57484092-C-G

199994225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57484734-T-C

199994414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57484914-T-C

199994673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57485163-A-G

199994734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57485222-T-C

199994793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57485279-C-T

199995957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57485987-T-G

199996038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486066-G-A

http://identifiers.org/hco/2/GRCh38#199996288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57486353-C-A

199996297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486362-G-A

199996336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486401-G-A

199996347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486412-C-T

199996515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486539-C-G

199996515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486539-C-T

199996613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486643-G-A

199996643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486673-G-A

199996798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486976-G-A

http://identifiers.org/hco/2/GRCh38#199996819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57486997-C-A

199996819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486997-C-G

http://identifiers.org/hco/2/GRCh38#199996846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57487022-C-A

199997125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487177-T-G

199997145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487196-G-A

199997145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487196-G-C

199997172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487234-C-T

199997187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487249-T-C

199997569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487596-C-T

199997755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487758-C-T

199997756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487759-T-C

199997781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487784-G-C

199997793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487796-C-T

199997823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487826-G-A

199997893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487869-T-A

199997927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57487893-G-A

199998099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488013-T-C

199998184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488082-T-C

199998382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488290-C-G

199998438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488356-T-C

199998634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488568-G-C

199998813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488744-G-C

199998968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488899-G-A

199999126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489068-T-C

199999211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489149-A-G

199999432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57489324-G-A

199999502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57489403-T-C

199999502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57489403-T-G

200000195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57491112-C-T

200000259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57491166-T-C

http://identifiers.org/hco/2/GRCh38#200000354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57491265-A-C

200000946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500312-C-T

200001173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500534-T-C

200001266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500628-G-A

200001340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500691-C-T

200001382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500733-G-C

http://identifiers.org/hco/2/GRCh38#200001506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57500842-C-A

200001557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500894-G-A

200001637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500975-C-T

200001939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57501464-G-T

200002131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57501636-A-G

200002386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57501888-T-C

200002400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57501902-C-T

200002893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502835-T-G

200002926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502866-C-T

200003173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503097-G-A

200003238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503156-A-G

http://identifiers.org/hco/2/GRCh38#200003600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#57503545-C-A

200003738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503682-T-C

200003879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503815-C-T

200004466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504395-T-C

200004664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504585-G-T

200004723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26198
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504644-C-G