102736915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5 prime UTR variant
orthologous variants: 40829901-G-C

102736915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5 prime UTR variant
orthologous variants: 40829901-G-T

102736930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5 prime UTR variant
orthologous variants: 40829903-C-T

http://identifiers.org/hco/2/GRCh38#102736959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40829932-C-A

102736959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40829932-C-T

102736996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40829951-G-A

102736996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40829951-G-T

102737000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 40829955-A-G

102737013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40829970-G-A

102737013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 40829970-G-T

102737030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40829978-T-C

102737101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830030-G-A

102737149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830072-A-G

102737215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830143-T-C

102737501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830407-G-C

102737504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40830410-C-G

102753708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40842077-T-C

102753845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40842206-A-G

102753917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40842270-A-G

http://identifiers.org/hco/2/GRCh38#102753925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40842278-C-A

102761064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40843837-G-C

http://identifiers.org/hco/2/GRCh38#102761126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40843906-A-C

102761160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40843943-C-T

102761255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844027-G-A

102761270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844042-A-G

102761326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844097-C-T

http://identifiers.org/hco/2/GRCh38#102761350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40844104-C-A

102761368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844120-T-G

102761380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844125-C-T

102761436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844174-T-C

102761518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844252-T-C

102761623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844361-A-T

102761880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844611-A-G

102761892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40844627-T-A

102762098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40844812-T-A

102762098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40844812-T-G

http://identifiers.org/hco/2/GRCh38#102762109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40844823-C-A

102762144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40844850-T-G

http://identifiers.org/hco/2/GRCh38#102762236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40844934-A-C

102762236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40844934-A-G

102762268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40844966-G-A

102762268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 40844966-G-T

102762390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845092-T-C

102762439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845135-G-A

102762460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845155-A-G

102762460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845155-A-T

http://identifiers.org/hco/2/GRCh38#102762472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40845167-C-A

102762472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845167-C-G

102762472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845167-C-T

102762476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845171-T-C

102762476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845171-T-G

http://identifiers.org/hco/2/GRCh38#102762797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40845454-A-C

102762811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845468-A-T

102762815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845472-G-A

102762815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845472-G-T

102762824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845478-T-C

102762828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845482-G-A

102762831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845485-A-G

102762896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845546-G-A

102763221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845887-A-G

102763227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40845893-G-T

102763368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846039-G-A

102763941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846431-G-A

102763946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846436-A-G

102764094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846577-T-C

102764094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846577-T-G

http://identifiers.org/hco/2/GRCh38#102764184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40846645-C-A

102764184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846645-C-T

102764236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846692-G-A

http://identifiers.org/hco/2/GRCh38#102764240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40846696-C-A

102764240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846696-C-T

http://identifiers.org/hco/2/GRCh38#102764264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40846718-C-A

102764264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846718-C-T

102764269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846723-A-G

102764271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846725-G-T

102764295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846748-A-G

102764375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40846828-G-A

102764375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40846828-G-T

102764470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846918-T-A

102764470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846918-T-C

102764556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846991-G-A

102764556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40846991-G-T

102764696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40847130-T-C

102764997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40847344-G-A

102764998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40847345-G-T

102765407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40847875-G-A

102765407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40847875-G-T

102765663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848111-A-G

http://identifiers.org/hco/2/GRCh38#102765687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40848135-C-A

102765687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848135-C-T

102765728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848173-A-T

102765738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848189-A-G

102765904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848326-C-G

102765905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848327-T-A

102766015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848421-C-T

102766508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40848902-C-T

102767041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849260-A-G

102767178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849463-C-G

102767278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849562-A-G

102767334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849619-C-T

102767521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849770-C-T

102767583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849829-G-A

102767583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40849829-G-C

102768709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40851083-T-A

102768786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40851156-G-A

102769108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40851654-G-T

102769122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40851668-A-G

102769129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40851674-A-G

102769426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40851973-A-G

102769570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40853748-A-G

http://identifiers.org/hco/2/GRCh38#102769574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40853752-C-A

102769574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40853752-C-T

102769734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40853918-G-A

102769772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40853952-A-G

102769780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40853961-G-A

102769869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854048-A-G

102769927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854111-A-G

102770048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854218-A-G

102770392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854557-A-G

102770395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854560-T-G

102770652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854830-G-T

102770755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854918-A-G

102770789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854950-T-C

102770800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40854961-C-T

102770857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855013-G-C

102770910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855066-G-T

http://identifiers.org/hco/2/GRCh38#102770940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40855088-A-C

102771023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855170-C-G

102771046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855188-T-C

102771121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855261-C-T

102771138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855273-A-G

102771286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855418-C-T

102771757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855813-G-A

102771926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40855993-G-A

102771977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40856058-T-C

102772564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857120-A-G

102772598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857156-C-T

102772689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857246-G-T

102772710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857259-G-C

102772750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857301-T-C

102772817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857365-T-G

102772879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857418-A-T

102773032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857567-G-A

102773116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857651-T-A

102773116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857651-T-C

102773188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40857728-G-A

102781916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40862182-T-C

http://identifiers.org/hco/2/GRCh38#102782925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40863655-C-A

http://identifiers.org/hco/2/GRCh38#102783213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40863930-C-A

102783558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40864279-C-G

102785106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40865665-A-G

102785113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40865672-C-T

102785319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40865882-C-T

102785390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40865958-G-C

http://identifiers.org/hco/2/GRCh38#102785434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40865990-A-C

102785434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40865990-A-G

102785751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40866258-A-G

102786115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40866655-A-G

102786320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40866682-T-A

102786548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40866781-C-T

102786703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40866928-A-G

http://identifiers.org/hco/2/GRCh38#102787083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40867371-C-A

102787455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40867717-A-G

102788558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40868380-G-A

102788576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40868398-G-A

102788605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40868427-C-G

http://identifiers.org/hco/2/GRCh38#102788611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40868433-A-C

102789110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40868895-G-C

102791413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40869871-T-C

http://identifiers.org/hco/2/GRCh38#102791440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40869898-C-A

102791499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40869953-C-T

102791530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40869983-T-G

102792304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40870269-C-T

102792526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40871717-C-G

http://identifiers.org/hco/2/GRCh38#102792594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40871784-C-A

102792595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40871785-A-G

102792670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40871880-C-T

102792706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40871915-G-A

102796632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40876292-C-T

http://identifiers.org/hco/2/GRCh38#102796789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40876447-C-A

102796789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40876447-C-T

http://identifiers.org/hco/2/GRCh38#102797559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40877164-C-A

102797583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40877188-C-T

102797624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877230-T-C

102797641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40877247-G-A

102797641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40877247-G-T

102797643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40877249-A-G

102797679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877284-A-G

102797683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40877288-A-G

102797702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877305-A-G

http://identifiers.org/hco/2/GRCh38#102797723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40877322-C-A

102797746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877354-A-G

102797752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877360-A-G

102797752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877360-A-T

102797753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877361-T-C

102797758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40877366-G-A

102797788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40877390-G-C

102797788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40877390-G-T

102797793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40877401-T-C

102797793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40877401-T-G

102797802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40877410-G-A

102798061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877652-T-G

102798190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877740-A-G

102798329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877863-G-A

102798407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40877913-A-G

102805532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883322-C-T

102805640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883419-A-G

102805719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883479-A-G

102805732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883492-A-G

102806029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883599-A-G

http://identifiers.org/hco/2/GRCh38#102806040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40883605-A-C

102806040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883605-A-G

102806081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883646-T-C

102806235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883801-G-A

102806289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883855-C-T

102806358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40883924-C-T

102806522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884269-G-A

102806536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884283-C-T

102806866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884641-G-A

102807175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884899-T-C

102807182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884906-G-A

102807182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884906-G-T

102807269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40884977-T-C

102807373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885066-A-G

102807442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885163-A-T

102807447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885173-A-G

102807647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885370-A-G

102807698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885422-A-G

102807736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885452-T-C

http://identifiers.org/hco/2/GRCh38#102807766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40885471-A-C

102807786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885490-A-G

102808191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40885756-G-A

102808417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40886091-G-A

102808475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40886128-C-T

102808488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40886140-C-T

102808560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40886186-T-C

102809261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40886798-C-T

102809340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40886892-A-T

102809572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887116-A-G

102809764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887483-A-G

102809774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887494-C-T

102809818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887536-G-A

102809880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887597-G-A

102809988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887696-T-C

102809990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40887698-G-A

102810894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40888928-A-G

102810894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40888928-A-T

102812327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40890086-T-C

http://identifiers.org/hco/2/GRCh38#102812476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40890207-A-C

102812946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40890667-T-C

102813040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40891322-A-G

102813120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40891400-C-T

102813268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40891543-C-T

102813362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40891624-A-G

102813379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40891641-C-T

http://identifiers.org/hco/2/GRCh38#102814071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40892850-A-C

102814623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40893840-G-C

102814640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40893857-A-G

102814640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40893857-A-T

http://identifiers.org/hco/2/GRCh38#102814668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40893876-C-A

102814668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40893876-C-T

102814900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894108-A-G

102814900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894108-A-T

102815020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894221-T-G

102815021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894222-T-A

http://identifiers.org/hco/2/GRCh38#102815064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40894269-A-C

102815100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894303-T-G

http://identifiers.org/hco/2/GRCh38#102815173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40894365-C-A

102815173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894365-C-G

102815173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894365-C-T

102815230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894414-T-C

102815242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894426-T-C

102815243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894427-G-C

102815243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894427-G-T

http://identifiers.org/hco/2/GRCh38#102815249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40894433-C-A

102815249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894433-C-G

102815249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894433-C-T

102815296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894467-G-A

102815296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894467-G-T

http://identifiers.org/hco/2/GRCh38#102815505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40894677-C-A

102815505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894677-C-T

http://identifiers.org/hco/2/GRCh38#102815530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40894701-A-C

102815530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894701-A-T

102815572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894739-G-T

102815760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894916-G-A

102815760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40894916-G-C

http://identifiers.org/hco/2/GRCh38#102815841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40894999-A-C

102815863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895021-A-G

http://identifiers.org/hco/2/GRCh38#102815872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40895030-C-A

102815872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895030-C-G

http://identifiers.org/hco/2/GRCh38#102815876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40895034-C-A

http://identifiers.org/hco/2/GRCh38#102815887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40895045-C-A

102815887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895045-C-G

102815957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895117-G-A

102815957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895117-G-T

102816013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895168-C-G

102816062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895217-T-C

102816190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895353-C-T

102816258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895444-C-T

102816266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895452-C-G

102816266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895452-C-T

102816300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895483-G-A

102816300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40895483-G-T

102816321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895503-C-T

102816334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895516-G-A

102816334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895516-G-T

102816403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895573-T-C

102816503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895667-G-A

102816574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895730-C-T

102816740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40895874-A-G

102816916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896050-T-G

102817045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896177-G-A

102817045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896177-G-T

http://identifiers.org/hco/2/GRCh38#102817282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40896387-A-C

102817422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896529-C-T

102817425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896532-C-T

102817642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896740-A-G

102817647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40896745-T-G

102817687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40896786-T-C

102817726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40896807-T-C

http://identifiers.org/hco/2/GRCh38#102817738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40896819-C-A

102817738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40896819-C-T

102817749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40896830-A-G

102818037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40897220-A-T

102818055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40897235-G-A

102818080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40897258-T-G

102818976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40900883-C-T

102819020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40900923-C-T

102819093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40900995-G-A

102819207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40901179-A-G

102819403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40901370-C-T

102819535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40901503-G-A

102825113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40904596-C-G

102825113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40904596-C-T

102826336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906293-T-A

102826345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906302-A-G

102826345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906302-A-T

102826426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906378-C-T

102826570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906506-C-T

102826712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906621-A-G

102826713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906622-C-T

102826802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906705-G-A

102826802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906705-G-C

102826831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40906734-T-C

102827023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40906909-C-T

102827026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40906912-G-A

102827026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40906912-G-T

102827031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40906917-T-A

102827042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40906928-G-T

102827255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40907128-T-C

102827340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40907215-A-G

102827426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40907300-T-C

http://identifiers.org/hco/2/GRCh38#102827499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40907382-A-C

http://identifiers.org/hco/2/GRCh38#102827530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40907413-C-A

102827732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40907609-T-C

102828748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40908302-A-G

102828807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40908361-G-T

http://identifiers.org/hco/2/GRCh38#102829483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40910872-A-C

102829593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40910980-C-T

102829642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40911050-A-G

102829644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40911052-C-G

102831783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40911897-T-A

102831783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40911897-T-G

102831808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40911920-T-G

102831920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40912018-A-G

http://identifiers.org/hco/2/GRCh38#102832470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40913011-A-C

102832787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913313-A-G

102832858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913384-T-A

102832974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913497-G-A

102832974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913497-G-C

http://identifiers.org/hco/2/GRCh38#102832986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40913509-C-A

102832986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913509-C-T

102833228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913745-T-C

102833341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40913852-C-T

http://identifiers.org/hco/2/GRCh38#102833386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40913897-C-A

http://identifiers.org/hco/2/GRCh38#102833387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40913898-A-C

102834739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916199-C-T

102834763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916222-G-A

102834844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916301-C-G

102834844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916301-C-T

102834965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916405-T-C

102835013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916455-T-C

102835013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916455-T-G

http://identifiers.org/hco/2/GRCh38#102835035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40916477-C-A

102835035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916477-C-T

http://identifiers.org/hco/2/GRCh38#102835066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40916507-A-C

102835123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40916570-T-C

102839998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40918247-G-T

102840156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40918446-C-T

102840481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40918757-G-T

102840509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40918784-A-T

102840905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40919437-A-G

102840988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40919521-T-G

102841074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40919601-A-G

102841357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40919845-T-G

http://identifiers.org/hco/2/GRCh38#102841460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40919941-C-A

102841551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920074-G-A

102841604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920226-G-T

102841721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920457-A-G

102841740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920478-G-A

102841777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920502-C-T

102841778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920503-G-A

102842033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920768-A-G

102842065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920800-C-T

102842287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40920982-C-T

102842375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40921040-A-G

102842485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40921122-T-A

102842581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40921209-G-A

102842581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40921209-G-T

102842859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40921927-C-T

102842871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40921944-C-T

102843411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 40922395-G-T

102843450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40922432-T-C

http://identifiers.org/hco/2/GRCh38#102843465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40922446-C-A

102843524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40922481-A-G

102843534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40922489-T-A

102843535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 40922490-G-A

102843604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40922558-G-A

102843604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40922558-G-C

102843604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40922558-G-T

102843650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40922604-T-C

102844030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40923039-A-G

102844372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40923346-A-T

102844499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40923459-A-G

102844499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40923459-A-T

102844610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40923553-A-G

102847436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40926559-A-G

102847582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40926705-T-A

102848671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40927100-G-C

102848682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40927111-C-G

102848682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40927111-C-T

102848690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40927119-C-G

102848779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40927227-A-G

http://identifiers.org/hco/2/GRCh38#102848857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40927328-A-C

102849096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40927586-C-G

http://identifiers.org/hco/2/GRCh38#102849229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40927707-A-C

http://identifiers.org/hco/2/GRCh38#102849321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40927784-C-A

102849659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928109-T-C

102849679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928128-G-C

102849750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928197-G-T

102849786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928233-G-A

102849831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928278-G-A

102849889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928337-C-T

102849894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928342-A-G

102850217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928659-C-T

http://identifiers.org/hco/2/GRCh38#102850274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40928718-C-A

102850400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928871-A-G

102850428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40928899-C-T

102850667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929136-T-G

102850673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929151-G-C

102850694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929185-G-A

102850715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929206-C-T

102850875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929379-A-G

102850884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929388-A-T

102851209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40929700-A-G

102851547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40930039-A-T

http://identifiers.org/hco/2/GRCh38#102851754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40930246-C-A

102851754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40930246-C-T

102851799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40930290-G-C

102851799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40930290-G-T

102852430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40931081-A-G

102852481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40931121-A-G

102852633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40931257-G-A

102852877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40931535-A-G

102855959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40931860-A-G

102856085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40931993-A-G

102856097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932005-G-A

102856128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932035-T-C

102856144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932051-G-T

102856177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932080-G-T

102856208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932114-G-A

102856258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932158-G-A

102856378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40932276-T-C

102857790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40933695-T-C

102857884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40933785-T-C

102860406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40936019-A-G

102860506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40936113-T-C

102860508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40936115-G-C

http://identifiers.org/hco/2/GRCh38#102860727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40936317-C-A

102861248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40936982-C-T

http://identifiers.org/hco/2/GRCh38#102861313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40937045-C-A

102861368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40937101-A-T

102861442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40937236-G-A

http://identifiers.org/hco/2/GRCh38#102861536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40937370-C-A

102861536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40937370-C-T

102861569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40937397-A-G

102861685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40937520-G-C

102861864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40937702-A-G

102862405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40938183-A-G

http://identifiers.org/hco/2/GRCh38#102862411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40938189-C-A

102864889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40939788-T-C

102864894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40939793-G-A

102864895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40939794-C-T

102864982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40939879-A-T

102865048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40939946-T-C

102865076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40939974-C-T

102865171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40940057-T-C

102865404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40940297-C-T

102865539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40940420-G-T

102865607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40940490-C-G

102865607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40940490-C-T

102868045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40941663-G-A

http://identifiers.org/hco/2/GRCh38#102869245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40943817-C-A

102869245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40943817-C-T

102869335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40943901-C-G

102869444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40943982-A-G

102869622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40945057-T-A

102869780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40945203-A-G

102870175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40945620-T-A

102870175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40945620-T-C

102870176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40945621-G-A

http://identifiers.org/hco/2/GRCh38#102870394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40945786-C-A

102872024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40947292-G-A

102872054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40947345-G-A

102872054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40947345-G-T

102872421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40947669-T-A

102872843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40948054-A-G

102873165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40948374-T-C

102873222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40948431-C-T

102873245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40948457-G-T

102873289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40948505-C-T

http://identifiers.org/hco/2/GRCh38#102873305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40948521-C-A

102873451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40948585-G-T

102873509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40948643-C-G

102873565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40948684-T-A

102873600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948753-G-T

102873601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948754-T-C

102873638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948795-G-A

102873638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948795-G-T

http://identifiers.org/hco/2/GRCh38#102873661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40948822-C-A

102873661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948822-C-T

102873665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948829-C-G

102873665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948829-C-T

http://identifiers.org/hco/2/GRCh38#102873683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40948847-C-A

102873689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948853-C-T

102873728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948888-T-C

102873747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40948907-A-G

http://identifiers.org/hco/2/GRCh38#102873799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40948935-C-A

102881361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949587-G-T

102881574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949808-G-A

102881621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40949846-A-G

102881782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950026-C-T

102881794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950038-T-C

http://identifiers.org/hco/2/GRCh38#102881796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40950040-C-A

102881949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950152-C-G

102881987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950190-A-G

102882125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950286-A-T

102882156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950306-T-A

102882349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950616-A-G

102882460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950835-G-T

http://identifiers.org/hco/2/GRCh38#102882610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40950982-A-C

102882610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40950982-A-T

102882756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951130-T-A

http://identifiers.org/hco/2/GRCh38#102882769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40951142-C-A

http://identifiers.org/hco/2/GRCh38#102882799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40951175-C-A

102882809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951185-A-G

102882835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951208-T-A

102882837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951231-T-A

102882849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40951243-C-T

102885636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953132-C-T

http://identifiers.org/hco/2/GRCh38#102885739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40953232-A-C

102885854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953331-A-G

102885910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953418-T-C

102886107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953832-T-C

102886107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40953832-T-G

102886394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40954100-G-A

102887545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40956438-C-T

102887806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40956652-T-C

102887937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40956772-G-A

102887971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40956806-G-C

102887971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40956806-G-T

102888395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957201-G-A

102888563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957363-C-T

102888644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957441-G-A

102888669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957466-G-A

102888844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957809-G-T

102888997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40957914-C-T

102889087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958003-C-G

102889099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958015-G-A

102889099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958015-G-T

102889109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958021-A-G

102889109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958021-A-T

102889117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958029-T-C

102889166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958078-T-G

102889192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958101-C-T

102889290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958218-G-A

102889293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958221-A-G

102889300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958228-C-T

102889339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958271-G-A

102889364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958288-T-C

http://identifiers.org/hco/2/GRCh38#102889382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40958306-A-C

102889443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958370-G-A

102889545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958467-T-C

102889572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958484-T-C

102889603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958516-C-T

102889626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958539-T-C

102889674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958586-T-G

102889865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40958757-A-G

http://identifiers.org/hco/2/GRCh38#102890239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40959130-A-C

102890390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40959263-C-G

102890700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961533-G-A

102890733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961569-G-T

102890736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961572-C-T

102890986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40961998-T-C

102891244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962272-A-G

102891313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40962341-A-T

102891331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40962359-A-G

http://identifiers.org/hco/2/GRCh38#102891403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40962432-C-A

102891467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962495-T-C

102891494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40962522-C-T

http://identifiers.org/hco/2/GRCh38#102892240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40963263-C-A

102892317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963339-T-G

102892417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963394-C-T

102892444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40963421-C-T

102892620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963532-C-T

102892875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963794-C-T

102892903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963820-T-C

102892929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963854-C-G

102892934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40963859-C-T

102893147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40964078-T-C

102893401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40964334-G-A

102893621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40964560-C-T

102900421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40967115-T-A

102900767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40967666-G-A

102900964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40967863-G-A

http://identifiers.org/hco/2/GRCh38#102901332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40968182-C-A

102903711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40970369-C-G

102904024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40970651-A-G

102904170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40970799-C-T

102904271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40970893-A-G

102905774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40973025-G-A

http://identifiers.org/hco/2/GRCh38#102905805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40973058-A-C

http://identifiers.org/hco/2/GRCh38#102905898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40973178-A-C

102905978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40973253-T-C

102906124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40973436-C-T

102906165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40973476-T-C

102906189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40973501-G-T

102906246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40973560-G-A

102906311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974298-C-T

102906323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974310-G-A

102906327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974314-C-T

102906433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974400-G-T

102906591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974541-T-A

102906646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974586-C-T

102906702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974636-C-T

102906853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40974785-A-G

102907632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40975854-G-A

102907632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40975854-G-T

102907652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40975874-G-T

102907874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40976090-G-A

102908010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40976224-T-G

102908011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40976225-A-G

102908381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40976606-A-G

102908474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40976702-G-A

102920150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40978679-A-G

102920222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40978750-G-A

102920886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40980801-G-T

102920915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40980830-G-A

102920954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40980897-A-T

102921076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981014-G-A

102921218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981144-A-T

102921226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981152-C-T

102921417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981339-A-G

102921494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981411-T-C

102921535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981445-T-C

102921726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981629-A-G

102921862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981764-C-T

102921890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981791-A-T

102921995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40981997-T-C

102922004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40982006-T-C

102922126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40982126-A-G

102922143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40982143-C-T

102922257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40982259-T-C

102922330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40982333-C-G

102923103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983132-A-G

102923234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983258-G-A

102923494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983512-G-A

http://identifiers.org/hco/2/GRCh38#102923582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40983603-C-A

102923582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983603-C-G

102923582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983603-C-T

102923732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983831-C-T

102923768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983867-G-A

102923989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983884-G-A

102923989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40983884-G-T

102924266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984080-C-G

http://identifiers.org/hco/2/GRCh38#102924350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40984173-C-A

102924350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984173-C-T

102924351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984174-G-A

102924546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984353-C-T

102924772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984588-C-T

102924955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984772-C-T

102925132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984950-T-C

102925172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984990-A-G

102925172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40984990-A-T

102925202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985020-G-T

102925242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985056-G-C

102925242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985056-G-T

102925250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985064-T-A

102925260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985074-T-C

102925340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985154-A-G

102925400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40985216-C-T

102928362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40989701-A-G

102928466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40989799-C-G

102928466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40989799-C-T

102928760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40989958-C-G

102929009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990212-T-C

102929009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990212-T-G

102929045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990249-C-T

102929212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990400-T-C

102929385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990563-G-A

102929497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990660-G-A

102929512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990673-A-G

102929528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990689-G-T

102929652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40990821-G-T

http://identifiers.org/hco/2/GRCh38#102929835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40991043-C-A

http://identifiers.org/hco/2/GRCh38#102929871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40991109-A-C

102929936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991200-C-G

102930865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991712-C-T

http://identifiers.org/hco/2/GRCh38#102930895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40991735-A-C

102930895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991735-A-G

102930895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991735-A-T

102930998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991839-A-G

102931022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991863-C-G

102931049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991887-T-G

102931092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40991939-A-T

http://identifiers.org/hco/2/GRCh38#102931126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40991967-C-A

102931211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40992029-T-C

http://identifiers.org/hco/2/GRCh38#102931256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40992074-A-C

http://identifiers.org/hco/2/GRCh38#102931780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40993251-C-A

102931804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40993281-T-A

102931810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40993287-A-T

102932069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40993547-C-T

102932223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40993709-G-A

102932230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40993716-C-G

102932797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40994287-T-A

102932797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40994287-T-C

102932843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40994333-T-C

102932890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, missense_variant
orthologous variants: 40994378-A-G

102932979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 40994467-T-C

102933003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 40994491-G-A

102933234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40994725-T-G

http://identifiers.org/hco/2/GRCh38#102933249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40994741-C-A

102933249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40994741-C-T

102933251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40994743-T-C

102933271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40994763-A-G

102933386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40994983-G-A

102933386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 40994983-G-T

102933535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40995187-G-T

102933565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40995212-A-G

102933641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40995292-G-A

http://identifiers.org/hco/2/GRCh38#102933704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40995347-C-A

http://identifiers.org/hco/2/GRCh38#102934271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40995850-C-A

102934271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40995850-C-T

102934420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40996766-A-G

102934451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40996843-C-T

102934513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40996898-G-A

102934513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40996898-G-T

102934755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40997132-G-C

102935008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40997370-T-C

http://identifiers.org/hco/2/GRCh38#102935770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40997735-C-A

102935770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40997735-C-T

102935776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40997741-T-G

102935981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40997944-G-A

102936225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40998168-C-T

102936450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40998382-T-C

http://identifiers.org/hco/2/GRCh38#102937103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#40999024-C-A

102937412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999345-A-T

102937542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999465-T-C

102937613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999537-A-G

102937622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999546-G-T

102937627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999551-T-G

102937736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999617-G-A

102937838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999746-T-C

102937873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999769-A-G

102937994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 40999891-A-G

102938173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41000070-A-G

102938173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41000070-A-T

http://identifiers.org/hco/2/GRCh38#102940738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41002939-C-A

102940738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41002939-C-T

102940914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003183-G-A

102941193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003447-T-C

102941213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003471-C-T

102941340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003689-C-T

102941456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003805-A-G

102941460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003809-T-A

102941540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003917-A-G

102941546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41003923-A-G

102941708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41004847-G-A

102941925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005035-A-T

102942048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005158-T-C

http://identifiers.org/hco/2/GRCh38#102942098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41005212-A-C

102942098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005212-A-T

102942167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005275-C-T

102942235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005328-A-G

102942244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005337-G-C

102942294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005381-G-T

102942350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005435-A-G

102942411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005481-C-G

102942416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005486-C-G

http://identifiers.org/hco/2/GRCh38#102942620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41005711-C-A

102942695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005785-C-T

102942705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005794-T-A

102942762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005850-G-A

102942762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005850-G-C

102942812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005904-T-C

102942895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005976-A-G

102942902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41005983-C-G

102943077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006144-C-T

102943102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006169-G-C

102943136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006203-A-G

102943138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006205-G-A

102943236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006284-T-C

102943281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006328-T-A

102943281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006328-T-C

102943642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006574-T-A

102943679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41006611-C-T

http://identifiers.org/hco/2/GRCh38#102944234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41007168-C-A

102944548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41007462-G-T

102944713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41007594-C-T

102944767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41007647-G-A

102944925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41007768-G-C

102944925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41007768-G-T

102945074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41007922-G-A

102945178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41008027-G-C

102945200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41008049-G-T

102945576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41008430-T-C

102945749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41008611-T-C

102945863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41008728-G-A

102945863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41008728-G-C

102946254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009124-G-T

102946406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009245-C-T

102946577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009399-G-A

102946630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009439-G-C

102946641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009447-G-T

102946859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009605-T-C

102946956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41009665-C-T

http://identifiers.org/hco/2/GRCh38#102947187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41009916-A-C

102947497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010229-T-C

102947561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010286-T-A

102947571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010296-T-G

102947715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010444-C-G

102947788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010509-A-G

102947874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010583-C-T

102947889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010598-G-A

102947924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010630-A-G

http://identifiers.org/hco/2/GRCh38#102947964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41010673-A-C

http://identifiers.org/hco/2/GRCh38#102947973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41010682-A-C

102947973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010682-A-G

102948163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010832-A-G

102948229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010890-C-T

102948348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41010988-A-G

102948368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41011005-T-A

102948406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41011057-A-G

102948724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41011389-A-T

102948777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41011436-C-T

102950428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41012359-T-G

102950460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41012390-A-G

102950514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41012439-C-T

102950521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41012446-C-T

102950696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41012629-G-T

102950698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41012631-C-T

http://identifiers.org/hco/2/GRCh38#102950702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41012635-C-A

102951120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013045-G-T

102951314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013231-A-G

102951316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013233-G-A

http://identifiers.org/hco/2/GRCh38#102951636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41013354-C-A

102951637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013355-T-A

http://identifiers.org/hco/2/GRCh38#102951731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41013445-A-C

http://identifiers.org/hco/2/GRCh38#102951836-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41013544-A-C

http://identifiers.org/hco/2/GRCh38#102951884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41013628-C-A

102952067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013803-T-C

102952167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013888-T-C

102952236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41013960-A-G

102952319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41014043-G-A

102952370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41014107-A-G

http://identifiers.org/hco/2/GRCh38#102954178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41017159-A-C

102954222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41017190-A-G

http://identifiers.org/hco/2/GRCh38#102954232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41017200-A-C

102954232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41017200-A-G

102956274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41019918-G-A

102956457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41020102-G-A

102958755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41023214-G-T

102958831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41023290-G-A

102958910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41023360-G-A

102959255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41023648-T-A

http://identifiers.org/hco/2/GRCh38#102959455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41023853-C-A

102959470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41023869-A-G

102959523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41023923-A-G

http://identifiers.org/hco/2/GRCh38#102962138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41025556-C-A

http://identifiers.org/hco/2/GRCh38#102962408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41025818-C-A

102962427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41025837-T-G

102962498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41025923-C-T

102962512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41025937-G-A

102962512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41025937-G-T

102962685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41026067-A-G

102962741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41026122-A-G

102962810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41026181-G-C

102962864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41026239-C-T

102962942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41026278-A-T

102963332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41027250-G-A

102963749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41027713-A-G

102963808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41027771-A-G

102964132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41028096-G-A

102964139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41028103-A-G

102964159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41028123-G-T

102964550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41028504-G-A

102965570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030446-T-C

http://identifiers.org/hco/2/GRCh38#102965603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41030479-A-C

102965603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030479-A-G

102965603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030479-A-T

102965670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: synonymous variant
orthologous variants: 41030545-T-C

http://identifiers.org/hco/2/GRCh38#102965724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41030599-C-A

102965724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: 3 prime UTR variant
orthologous variants: 41030599-C-T

102965741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41030615-T-C

http://identifiers.org/hco/2/GRCh38#102965746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41030620-C-A

102965746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030620-C-G

http://identifiers.org/hco/2/GRCh38#102965783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41030649-C-A

102965783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030649-C-G

102965783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030649-C-T

102965795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030660-G-T

102965822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030699-G-A

102965878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030756-A-G

102965905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030779-T-C

102967252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030831-G-A

102967270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030849-G-A

102967270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030849-G-T

102967312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030891-G-A

102967312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030891-G-C

102967312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41030891-G-T

102967450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41031007-T-C

102967613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031155-G-T

102967736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031267-T-C

102967756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031287-T-C

102967926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031577-G-A

102967982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031628-G-C

102968036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031680-A-T

102968129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031773-G-C

102968293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41031938-C-T

102968519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032171-C-T

102968685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032337-G-C

102968866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032520-G-C

http://identifiers.org/hco/2/GRCh38#102968902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41032540-C-A

102968929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41032568-G-T

102968980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41032617-G-T

102969065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032699-G-T

http://identifiers.org/hco/2/GRCh38#102969163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41032782-C-A

102969293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032880-C-T

102969360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41032946-A-T

102969665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033372-T-G

102969850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033578-A-T

102969935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033660-A-G

102970244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41033968-G-A

102970342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034056-G-T

102970343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034057-A-G

102970470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034166-C-T

102970661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034350-T-C

102970683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034372-T-C

http://identifiers.org/hco/2/GRCh38#102970836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41034528-C-A

102970836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034528-C-T

102970837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41034529-T-G

102970951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41034645-T-C

102970994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41034683-C-T

http://identifiers.org/hco/2/GRCh38#102971321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41034972-A-C

102971587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035578-G-A

102971666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035657-T-C

102971837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035820-T-C

102971897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035881-A-G

102971976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035960-A-T

102971983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035967-A-G

102972008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035992-A-G

102972276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036263-T-G

102972302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036296-G-T

102973291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038442-T-C

102973659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038796-G-A

http://identifiers.org/hco/2/GRCh38#102973684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41038821-A-C

102973684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41038821-A-G

102974008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039104-T-A

102974008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039104-T-C

102974388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039121-C-G

102974545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039264-T-C

102974545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039264-T-G

102974703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039408-C-G

102974716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039422-G-A

102974741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41039447-A-G

102975281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040007-G-A

102976097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040773-T-G

102976165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040875-C-T

102976193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040904-C-T

102976265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040971-A-G

102976445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041149-T-C

102976494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041198-C-T

http://identifiers.org/hco/2/GRCh38#102976897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41041615-A-C

102976976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041698-G-A

102977093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041811-G-A

102977103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041819-G-A

102977208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041912-T-G

102977274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041968-G-A

http://identifiers.org/hco/2/GRCh38#102977418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41042100-C-A

102977418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41042100-C-T

102977547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41042215-G-A

http://identifiers.org/hco/2/GRCh38#102977744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41042393-A-C

http://identifiers.org/hco/2/GRCh38#102977960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41042606-C-A

102978104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41042687-A-G

102978105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41042688-G-T

http://identifiers.org/hco/2/GRCh38#102978181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41042762-C-A

102978484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043074-C-T

102978534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043139-T-C

102978610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043207-C-T

102978772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043442-C-T

102978786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043493-T-C

102978924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043720-T-C

102978956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043752-T-C

102978984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043780-G-A

102979202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044326-T-A

102979252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044373-G-A

102979602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044909-A-T

102979714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045033-A-G

102979778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045075-G-A

102979953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045221-T-C

102980024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045340-C-T

102980083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045396-C-T

102982226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045529-G-T

102982295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045560-G-A

102982328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045587-T-C

102983715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046039-G-A

102983715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046039-G-T

102983866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046193-G-A

102984025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046353-C-T

102984312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046640-G-T

102984334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046662-A-G

102984334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046662-A-T

102984457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41046790-A-G

102984536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41046869-T-C

http://identifiers.org/hco/2/GRCh38#102984538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41046871-C-A

102984538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41046871-C-G

102984841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41047119-T-C

102984841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41047119-T-G

102985615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048477-C-T

102985640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048501-A-G

102985687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048577-C-T

102985718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048608-T-C

102985741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048629-C-T

102985861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048748-T-C

102985887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048773-C-T

102986096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048976-A-G

102986113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41048993-A-G

102986134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049014-T-G

102986139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049019-T-A

102986659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049205-T-C

102986717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049265-T-A

102986756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049303-A-T

102987291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049766-A-G

102987292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41049767-G-A

http://identifiers.org/hco/2/GRCh38#102987357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41049828-C-A

102987357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41049828-C-T

http://identifiers.org/hco/2/GRCh38#102987375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41049845-C-A

102987375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41049845-C-G

102987470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41049926-T-C

102987566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41050006-G-T

http://identifiers.org/hco/2/GRCh38#102987589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41050029-A-C

102987641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050081-T-C

102987660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050096-C-T

102987954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41050279-C-T

102988207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41050507-G-T

102988294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41050567-A-G

http://identifiers.org/hco/2/GRCh38#102988577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41050801-C-A

http://identifiers.org/hco/2/GRCh38#102988688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41050900-C-A

102988708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41050916-A-G

102988892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41051104-C-T

http://identifiers.org/hco/2/GRCh38#102988979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41051175-A-C

http://identifiers.org/hco/2/GRCh38#102989152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41051346-C-A

102989260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41051446-C-G

102989393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41051574-T-A

102989421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41051602-A-G

102989811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41051785-T-C

http://identifiers.org/hco/2/GRCh38#102990213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41052154-A-C

102990214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41052155-C-T

102990413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41052314-G-T

102990477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41052351-T-C

102990483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41052357-T-C

102993040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41055641-A-T

102993111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41055711-A-G

102993165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41055766-T-C

102993241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41055823-G-A

102993490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056042-C-T

http://identifiers.org/hco/2/GRCh38#102993497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41056049-A-C

102993521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056069-C-T

102993524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056072-G-A

102993584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056121-T-C

102993598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056136-T-A

102993635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056175-T-C

102993703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056261-G-A

102993827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056387-C-T

102993859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056423-A-T

102993887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056448-A-G

http://identifiers.org/hco/2/GRCh38#102993917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41056478-A-C

102993927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056487-T-A

102993927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056487-T-G

102994072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056617-T-G

102994159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056702-G-C

102994159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41056702-G-T

102994361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41057011-T-A

102994817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41057458-C-T

103002342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065080-A-G

http://identifiers.org/hco/2/GRCh38#103002491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41065233-C-A

103002511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065243-G-A

103002684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065416-G-A

103002849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065578-G-A

103002933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065702-G-A

103002964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065735-C-T

http://identifiers.org/hco/2/GRCh38#103002969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41065740-C-A

103002969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065740-C-G

103002969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065740-C-T

103002970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065741-G-A

103002970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065741-G-T

103002974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065747-G-A

103003102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065872-A-G

103003122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41065892-C-T

103003236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066003-T-G

103003342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066109-G-T

103003566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066347-G-A

103003566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066347-G-T

103003796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066584-T-C

103003863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066668-A-T

103003930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41066732-C-T

103004203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067004-T-C

103004228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067029-G-A

103004345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067146-C-T

http://identifiers.org/hco/2/GRCh38#103004385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41067210-C-A

103004385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067210-C-G

103004387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067212-T-A

103004397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067222-A-G

103004460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067314-G-A

103004777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067640-G-T

103004796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067659-T-A

103004796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067659-T-C

103004796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067659-T-G

103004868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067777-G-A

103004868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067777-G-T

103005027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067939-A-G

103005070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067975-C-G

103005091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41067995-T-C

103005336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41068207-T-C

103005675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41068421-G-A

103006116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41068807-G-T

103006233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41068920-C-G

103006327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41068992-A-G

103006386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069060-T-C

103006622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069293-C-T

103006707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069380-T-C

http://identifiers.org/hco/2/GRCh38#103006781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41069454-C-A

103006817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069493-C-T

103006872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069548-C-T

103007031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069710-A-G

103007125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41069885-A-G

103007752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41072334-G-A

http://identifiers.org/hco/2/GRCh38#103007990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41072534-A-C

103008143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41072687-T-A

http://identifiers.org/hco/2/GRCh38#103008183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41072726-C-A

http://identifiers.org/hco/2/GRCh38#103009138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41073396-A-C

103009139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41073397-A-T

103009426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41073709-C-T

103009568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41073850-T-G

103009605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41073886-G-A

103009915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41074208-G-A

103009937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41074230-G-A

103010343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41074630-C-G

103010673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41074958-A-G

103010707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41074994-C-T

103010763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41075051-G-T

http://identifiers.org/hco/2/GRCh38#103011022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41075515-C-A

103011284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41075779-T-A

103011496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41076020-T-C

103011717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41076198-A-G

103011717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41076198-A-T

103011763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron variant
orthologous variants: 41076260-C-T

103011781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41076288-C-T

103011849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41076359-A-G

http://identifiers.org/hco/2/GRCh38#103012057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41076541-C-A

103012057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41076541-C-T

103012161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41076631-C-T

103012373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41076786-C-T

103012443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41076843-G-T

103012448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41076848-T-G

103012664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077291-C-G

103012718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077364-G-A

103012951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077581-C-T

103012991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077620-G-A

103013036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077661-C-T

103013313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077771-G-T

103013339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077796-G-A

103013422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077881-A-G

103013422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077881-A-T

103013441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077898-C-T

103013480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077940-T-C

103013485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077945-G-A

103013510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41077999-A-G

103013900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 41078534-T-G

103013945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41078580-A-G

http://identifiers.org/hco/2/GRCh38#103013947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41078582-A-C

103013947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41078582-A-G

http://identifiers.org/hco/2/GRCh38#103014109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41078756-A-C

103014989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41079386-C-T

http://identifiers.org/hco/2/GRCh38#103015035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#41079430-A-C

103015035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41079430-A-G

103015227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41080068-G-A

103015243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41080084-A-T

103015869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41080675-G-A

103016267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081086-T-A

103016267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081086-T-C

103016563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081379-A-T

103016596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081411-A-G

103016813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081668-A-G

103016991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081862-C-T

103016994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081865-C-T

103017001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41081872-A-G