93451712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121503-G-A

93451712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121503-G-C

93451712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121503-G-T

93451803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121413-T-C

93451803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121413-T-G

93451899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121323-G-A

93451899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121323-G-C

93451899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49121323-G-T

http://identifiers.org/hco/9/GRCh38#93452447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49120655-C-A

93452447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49120655-C-T

93452514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49120455-C-G

93452514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49120455-C-T

93452584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49120307-C-G

93452584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 49120307-C-T

93452609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49120276-G-A

93452609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49120276-G-T

93452902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119993-G-A

93452903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119992-T-C

http://identifiers.org/hco/9/GRCh38#93453037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49119859-A-C

93453037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119859-A-G

93453232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119674-G-T

http://identifiers.org/hco/9/GRCh38#93453269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49119635-C-A

93453304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119600-G-A

93453339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119568-C-G

93453339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49119568-C-T

93453699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49119208-G-A

93453699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49119208-G-T

http://identifiers.org/hco/9/GRCh38#93453709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49119198-C-A

93453709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49119198-C-T

93453729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49119179-A-G

93453773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49119136-T-G

93453856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49119056-C-T

93455614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49116995-G-A

93456237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49116607-A-G

93459563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49113644-C-T

93459684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, undefined
orthologous variants: 49113433-T-G

93460162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49113056-A-G

93460186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49113036-T-C

93460657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49112440-T-C

93460712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49112381-A-T

93463092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49110790-C-T

93463143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49110743-G-A

93463586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49110291-C-T

93463611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49110266-A-G

93464517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49108525-C-G

93464517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49108525-C-T

93465046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49106579-G-A

93469857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49103889-T-C

93469857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49103889-T-G

93471133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 49102789-T-C

http://identifiers.org/hco/9/GRCh38#93471466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49102474-C-A

93471466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49102474-C-T

93471482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49102458-A-T

http://identifiers.org/hco/9/GRCh38#93471521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49102432-C-A

93471521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49102432-C-T

http://identifiers.org/hco/9/GRCh38#93471532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49102421-C-A

93471588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49102356-T-G

93471673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49102278-A-G

93471809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49101697-C-T

93475439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49100147-T-C

93475789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099889-T-C

93476203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099550-T-G

93476222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099532-G-A

93476291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49099463-T-C

93476376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099383-A-G

93476384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099375-T-A

93476419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099340-T-C

93476476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099279-G-A

93476476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099279-G-T

93476484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099271-T-C

93476497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49099262-A-G

http://identifiers.org/hco/9/GRCh38#93477098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49098704-C-A

93477266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49098529-C-T

93477924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49097775-A-T

93478020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49097677-T-C

93478045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49097649-T-A

93479040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49096935-T-C

93479130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49096866-G-A

93479656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49096496-C-T

http://identifiers.org/hco/9/GRCh38#93479700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49096453-A-C

93479700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49096453-A-G

93481191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49094982-C-T

93481275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49094896-A-G

93481444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49094763-C-T

http://identifiers.org/hco/9/GRCh38#93483074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49094247-A-C

93483386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49093960-T-G

93483966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49093462-A-T

93490591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49090891-T-C

93490693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49090813-T-C

93490870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49090673-C-G

93491762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49089682-T-C

93496644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49088248-A-G

93496740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49088154-G-A

93496755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49088139-G-A

93496755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49088139-G-C

93497340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49087682-A-G

93497507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49087516-G-A

93497507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49087516-G-C

http://identifiers.org/hco/9/GRCh38#93498692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49085955-C-A

93498692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49085955-C-T

93498898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49085759-A-G

93500045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49084896-G-A

93500152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49084804-C-T

93500171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49084785-T-C

93500443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49084524-C-T

93513011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076886-C-T

93513030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076870-T-C

93513552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076363-T-C

93513707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076210-T-C

93513756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076164-G-A

93513786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076133-C-G

93513854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49076038-G-A

http://identifiers.org/hco/9/GRCh38#93515605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49075789-A-C

93515605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49075789-A-G

93515605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49075789-A-T

93515839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49075578-C-T

93516008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49075414-G-A

93516008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49075414-G-T

93516157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49075268-C-T

93516467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49075038-T-C

http://identifiers.org/hco/9/GRCh38#93516945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49074633-A-C

93517054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49074491-G-A

93517349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49074332-A-G

93517379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49074301-A-G

93517524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49074173-G-C

93517605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49074133-A-G

93517888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49073927-G-T

93517909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49073911-C-T

93518243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49073620-A-G

93522114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49072261-C-G

93522127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49072247-T-C

93522701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49071624-G-A

93525053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49070255-A-T

93526119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49069197-G-A

http://identifiers.org/hco/9/GRCh38#93527103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49068472-C-A

93527103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49068472-C-G

93527103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49068472-C-T

93527135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49068442-C-T

93527252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49068326-C-G

93528581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49067325-G-A

93529641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 49066287-T-A

http://identifiers.org/hco/9/GRCh38#93529799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49066125-C-A

93529799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49066125-C-T

93529961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49065980-T-G

http://identifiers.org/hco/9/GRCh38#93530014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49065936-C-A

93530014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49065936-C-T

93530112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49065839-T-G

93530405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49065585-G-C

93530929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49065132-A-G

93531008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49065055-G-T

93531352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 49064699-G-T

93531538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49064535-C-T

93531889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49064162-C-T

93532472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 49063590-G-A

93532590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49063482-T-C

93532654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49063416-G-T

93532673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49063401-T-C

93532685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49063389-G-T

93532872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49063277-C-T

93533304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49062889-A-G

93534078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49062382-C-T

93534770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49061785-G-A

93535053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49061524-A-T

93538022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49059807-T-A

93538257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49059611-A-G

93540196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49058238-G-A

93540196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49058238-G-C

93540311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49058122-G-A

93540335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49058097-T-A

93540922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49057676-C-T

93541286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49057397-T-C

93541286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49057397-T-G

93541350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49057315-G-A

93541744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056865-T-C

93541884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056760-C-T

http://identifiers.org/hco/9/GRCh38#93541978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49056673-C-A

93542496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056400-T-C

93542673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056237-T-G

93542763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056156-A-G

93542849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056081-G-A

93542866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49056064-G-A

93543107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49055892-T-A

93543107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49055892-T-C

93543550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49055484-A-G

93543597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49055431-G-A

93547916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49053036-C-G

93549403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49052133-A-T

93550488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49051327-G-A

93550488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49051327-G-T

93550531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49051287-G-A

93550531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49051287-G-T

93550974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49050874-A-G

93551496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49050387-A-T

93551864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49050052-C-G

http://identifiers.org/hco/9/GRCh38#93552527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49049453-A-C

http://identifiers.org/hco/9/GRCh38#93553535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49048455-C-A

93553535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49048455-C-G

93553535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49048455-C-T

93553929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49047758-T-G

http://identifiers.org/hco/9/GRCh38#93554182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49047471-A-C

93554182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49047471-A-T

93554301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49047360-C-T

93554974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49046826-C-T

http://identifiers.org/hco/9/GRCh38#93555117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49046697-A-C

93556010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49045902-T-C

93556086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 49045832-C-T

93556597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49045349-C-T

http://identifiers.org/hco/9/GRCh38#93557747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49043487-C-A

93557747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49043487-C-G

93558369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042939-G-A

93558370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042938-T-C

93558456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042858-G-T

http://identifiers.org/hco/9/GRCh38#93558475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49042839-C-A

93558475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042839-C-T

93558496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042818-G-C

93558496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042818-G-T

93558497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042817-G-A

http://identifiers.org/hco/9/GRCh38#93558503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49042811-C-A

93558503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042811-C-G

93558649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron_variant, missense_variant
orthologous variants: 49042667-G-A

93558850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042466-G-A

93558850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49042466-G-T

93561045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49039458-T-C

93561337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49039128-A-G

93561791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49039071-A-G

93561834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49039021-G-A

93562350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49038715-A-G

http://identifiers.org/hco/9/GRCh38#93562432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49038639-C-A

93562432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49038639-C-T

http://identifiers.org/hco/9/GRCh38#93562450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49038621-C-A

93562450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49038621-C-T

93563741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49035030-T-G

93563752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49035019-C-T

93563791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49034975-C-T

93563839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: intron variant
orthologous variants: 49034923-T-C

93564334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: missense variant
orthologous variants: 49034476-G-A

93564622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3 prime UTR variant
orthologous variants: 49034192-G-A

93564622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3 prime UTR variant
orthologous variants: 49034192-G-T

http://identifiers.org/hco/9/GRCh38#93564783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#49034020-C-A

93564811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3 prime UTR variant
orthologous variants: 49033993-T-A

93564811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3 prime UTR variant
orthologous variants: 49033993-T-C

93565608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13247
most severe consequence: 3 prime UTR variant
orthologous variants: 49033200-T-C