http://identifiers.org/hco/1/GRCh38#84298367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146391363-C-A

http://identifiers.org/hco/1/GRCh38#84298443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146391282-C-A

84298488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 146391236-G-A

84298488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 146391236-G-C

84298488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 146391236-G-T

84298506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 146391223-T-C

84298515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 146391214-G-T

84298610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146391149-G-A

84298610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146391149-G-C

84298610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146391149-G-T

84298629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146391134-A-G

84298629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146391134-A-T

84298663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146391074-G-A

84298663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146391074-G-T

84298718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146391033-T-C

84298718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146391033-T-G

84298755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390996-G-C

84298756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390995-T-C

84299126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390779-G-A

84299226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390701-T-G

84299320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390620-C-T

84299338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146390602-G-A

84299411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390558-T-C

http://identifiers.org/hco/1/GRCh38#84299441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146390534-C-A

84299441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146390534-C-T

84299444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146390531-G-A

84299444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 146390531-G-T

84299463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390512-G-T

84299612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 146390385-G-T

84299657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390344-G-A

84299657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390344-G-C

84299657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390344-G-T

http://identifiers.org/hco/1/GRCh38#84299667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146390334-A-C

84299667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390334-A-G

84299669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390332-A-G

84299669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390332-A-T

84299946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146390151-C-T

84300142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389977-A-G

84300312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389816-A-G

84300454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389654-T-C

84300517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389596-T-G

84300787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389040-C-T

84300792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389035-C-T

84300801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146389026-T-C

84300866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146388982-G-A

84301383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146388494-T-A

84301497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146388390-A-G

84301565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146388321-G-T

http://identifiers.org/hco/1/GRCh38#84301572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146388313-C-A

84301572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146388313-C-T

84301624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, undefined
orthologous variants: 146388260-T-C

84301880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387985-G-A

84301880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387985-G-T

http://identifiers.org/hco/1/GRCh38#84301884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146387981-C-A

84301884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387981-C-T

84301904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387961-G-A

84301904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387961-G-C

84301904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387961-G-T

84301965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387904-A-G

84301984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387885-G-A

84301992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387877-A-G

84301999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146387810-T-C

http://identifiers.org/hco/1/GRCh38#84302177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146387613-A-C

http://identifiers.org/hco/1/GRCh38#84302524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146387282-C-A

http://identifiers.org/hco/1/GRCh38#84302563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146387244-C-A

84302563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146387244-C-T

http://identifiers.org/hco/1/GRCh38#84302596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146387196-C-A

84302600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146387192-G-T

84302609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146387127-G-A

84302609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146387127-G-T

84302639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146387081-C-T

84302725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146386999-T-C

http://identifiers.org/hco/1/GRCh38#84302770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146386970-A-C

http://identifiers.org/hco/1/GRCh38#84302823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146386942-A-C

84302823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146386942-A-G

84302823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146386942-A-T

84302931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146386841-G-T

http://identifiers.org/hco/1/GRCh38#84302934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146386838-C-A

http://identifiers.org/hco/1/GRCh38#84303011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146386771-C-A

84303030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146386754-G-A

84303030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146386754-G-T

84303058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 146386726-A-G

84303076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 146386710-G-T

http://identifiers.org/hco/1/GRCh38#84303327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146386475-A-C

84303327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386475-A-G

84303360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386442-T-C

84303385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386423-T-G

84303387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386421-G-T

84303517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386296-A-T

84303581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386235-C-G

84303617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386197-G-T

84303650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386162-G-T

84303687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386126-A-G

84303688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386125-T-C

84303692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386122-G-T

84303765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386047-G-A

84303765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386047-G-T

84303802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146386012-T-G

84303912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385869-G-A

84303950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385848-A-G

84303988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385810-G-A

84304038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385775-A-G

84304125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385726-C-T

84304162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385689-G-T

84304236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385616-A-G

84304247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385605-G-T

84304250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146385604-A-G

84304482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146385164-T-C

84304544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146385098-T-G

84304558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146385072-T-G

http://identifiers.org/hco/1/GRCh38#84304673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146384957-C-A

84304673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146384957-C-T

84304927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146384501-A-G

http://identifiers.org/hco/1/GRCh38#84305175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146384288-A-C

84305469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146383965-G-A

84305648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146383816-G-T

84305676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146383754-T-C

84305680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146383662-G-C

84305816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146383410-T-C

84307749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146382942-T-C

http://identifiers.org/hco/1/GRCh38#84307878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146382822-C-A

84307985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146382720-G-A

84308073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146382635-A-G

84308153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146382534-T-C

84308163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146382524-T-C

http://identifiers.org/hco/1/GRCh38#84308176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146382512-A-C

84308471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146382236-A-G

84309285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146380980-G-C

84309784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146380383-A-G

http://identifiers.org/hco/1/GRCh38#84309894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146380160-C-A

84309894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146380160-C-T

84310047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379962-A-G

84310241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379772-T-C

84320078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379635-G-A

84320198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379469-A-G

84320242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379422-A-T

84320307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379336-A-T

84320437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379207-C-T

84320439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379205-G-C

84320522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146379121-G-A

84320671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146378967-T-C

84320870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146378760-T-C

84320880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146378751-T-C

http://identifiers.org/hco/1/GRCh38#84321049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146375826-A-C

84321334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146375480-T-A

84321423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146375394-T-G

84321569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146375268-A-G

http://identifiers.org/hco/1/GRCh38#84321755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146375093-C-A

84321755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146375093-C-T

84321822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146375048-T-A

http://identifiers.org/hco/1/GRCh38#84321847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146375025-C-A

http://identifiers.org/hco/1/GRCh38#84321905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146374970-C-A

84322941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146372607-T-A

84323374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146372224-C-T

84323988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146370106-C-T

http://identifiers.org/hco/1/GRCh38#84324292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146369814-A-C

84324371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146369736-T-C

84324599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146369535-C-G

84324599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146369535-C-T

84324682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146369405-G-A

84324813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146369306-C-G

84325030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146369105-G-A

84325151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368986-G-A

84325418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368813-C-T

84325572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368593-T-A

84325659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: missense variant
orthologous variants: 146368513-C-G

84325757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368415-G-T

http://identifiers.org/hco/1/GRCh38#84325770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146368364-C-A

84325770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368364-C-T

84325776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368353-G-A

84325783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368346-T-G

http://identifiers.org/hco/1/GRCh38#84325813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146368159-C-A

84325813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368159-C-G

84325813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368159-C-T

84325907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368072-C-T

84325938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146368042-A-G

http://identifiers.org/hco/1/GRCh38#84326122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146367879-A-C

84326122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367879-A-G

84326124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367874-A-G

84326157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367841-G-A

84326215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367793-G-A

84326231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367777-C-T

84326299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367696-A-G

84326361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367631-A-G

84326513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367490-G-T

84326534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367468-G-A

84326825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367249-A-G

84326832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367245-A-G

84326992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146367095-G-A

84327174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146366916-T-C

84327241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146366848-T-A

84327472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146366632-A-G

84327533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146366568-G-T

84327674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146365786-G-A

84327716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146365762-A-T

http://identifiers.org/hco/1/GRCh38#84328049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146365458-A-C

84328144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146365371-C-T

84328482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146365080-G-A

84328608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364957-G-T

84328785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364803-G-A

84328815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364781-G-A

84328815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364781-G-T

84328866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364732-T-C

84328960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364638-C-T

84329097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364501-T-G

84329902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146364107-T-A

84330052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363978-G-A

84330052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363978-G-T

84330164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363892-A-G

84330299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363761-T-C

84330391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363701-G-C

84330525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363615-G-A

84330525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363615-G-C

84330888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146363250-T-C

http://identifiers.org/hco/1/GRCh38#84331352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146362841-A-C

84331352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146362841-A-T

http://identifiers.org/hco/1/GRCh38#84331460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146362720-A-C

84339730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146361284-T-C

84339847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146361170-T-C

http://identifiers.org/hco/1/GRCh38#84339955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146361068-C-A

84339955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146361068-C-G

84340217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146360789-C-T

84340280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146360741-G-A

84340289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146360732-A-G

84340702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146360025-G-A

84340800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146359962-A-G

84340973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146359529-C-T

84341047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146359454-C-G

84341391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146359121-A-G

84341559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146358976-G-A

84341615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146358925-G-A

84341707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146358848-G-A

84341729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146358826-G-A

84341756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146358810-A-T

84342088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146358546-G-C

84344584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146357000-A-T

84344588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146356996-G-A

84344717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146356865-G-A

84344717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146356865-G-T

http://identifiers.org/hco/1/GRCh38#84344750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146356832-C-A

84344945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146356601-G-T

http://identifiers.org/hco/1/GRCh38#84344985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146356520-C-A

84344985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146356520-C-T

84344994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146356511-G-A

http://identifiers.org/hco/1/GRCh38#84345084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146356421-A-C

84345265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146356236-A-G

84345329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146356175-G-T

84345385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146356127-G-T

84345630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146355949-T-C

84345717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146355865-C-G

84346512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146355321-T-C

84346615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146355216-T-A

84346618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146355213-C-T

84346875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354987-T-A

http://identifiers.org/hco/1/GRCh38#84346908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146354964-A-C

84346916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354956-G-A

84347184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354641-A-T

84347355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354496-A-G

84347594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354270-C-T

84347754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354014-G-A

84347754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146354014-G-C

84347779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353989-G-A

http://identifiers.org/hco/1/GRCh38#84347860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146353885-A-C

84347995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353751-G-A

http://identifiers.org/hco/1/GRCh38#84348266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146353508-C-A

84348266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353508-C-T

84348362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353418-G-A

84348362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353418-G-T

84348424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353361-A-G

84348651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353183-C-T

84348747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353103-T-C

84348795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353074-A-G

84348857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146353027-G-C

84348913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146352971-G-A

84349002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146352895-G-T

http://identifiers.org/hco/1/GRCh38#84349252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146352542-A-C

84349355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146352437-T-C

84349504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146352303-A-G

84349525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146352288-G-C

84349591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146352226-T-A

84349689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 146352124-A-T

84349813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146352005-A-G

http://identifiers.org/hco/1/GRCh38#84349966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146351853-A-C

http://identifiers.org/hco/1/GRCh38#84349971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146351848-C-A

84349971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351848-C-T

84350087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351737-T-G

84350140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351683-G-C

84350183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351639-A-G

84350184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351638-A-G

84350315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351464-C-T

84350339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351438-A-T

84350694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146351048-G-A

84350798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 146350946-A-G

84350878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146350870-G-A

84350878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146350870-G-C

84351047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146350581-G-A

84351753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146349578-G-A

84351855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146349471-T-C

84351859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146349467-G-A

84351907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146349421-C-G

84352151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146349183-T-G

84352209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146349124-G-A

84353263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146348406-C-G

84353263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146348406-C-T

84353802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146348116-G-A

http://identifiers.org/hco/1/GRCh38#84353853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146348065-C-A

84353916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146347998-C-T

84356050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146347288-C-G

http://identifiers.org/hco/1/GRCh38#84356107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146347229-A-C

http://identifiers.org/hco/1/GRCh38#84356180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146347172-C-A

84356307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146347058-G-A

84356428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146346969-G-T

84356735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146346683-G-A

84356934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146346506-C-T

84357200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146346239-C-T

84357499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146345960-T-C

84357505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146345954-T-C

84357591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146345880-C-T

84357764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146345722-C-T

84357814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146345699-T-A

84362290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146343463-T-G

84362373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146343376-C-T

84362619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146340857-T-C

http://identifiers.org/hco/1/GRCh38#84362665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146340820-C-A

84362665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146340820-C-G

84362687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146340799-G-A

84362766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146340736-A-G

http://identifiers.org/hco/1/GRCh38#84363024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146340502-C-A

84363253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146339918-C-T

84363495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron variant
orthologous variants: 146339711-A-G

84364467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146337703-A-G

84364521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146337646-A-G

http://identifiers.org/hco/1/GRCh38#84364602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146337564-C-A

84364667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146337499-C-T

84364876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146337277-G-A

84365109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146336649-G-T

84365449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146336332-A-G

84365693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146336105-A-T

84365730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146335487-T-C

84365840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146335383-G-A

84365840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 146335383-G-C

84366288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334819-C-T

84366450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334666-C-T

84366807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334350-G-A

84366807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334350-G-C

84366807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334350-G-T

84366846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334312-T-C

84366977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334241-G-C

http://identifiers.org/hco/1/GRCh38#84367589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333698-A-C

84367589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333698-A-G

84367727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146333567-T-C

84367773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333521-A-G

http://identifiers.org/hco/1/GRCh38#84367775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333519-C-A

http://identifiers.org/hco/1/GRCh38#84367812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333486-C-A

http://identifiers.org/hco/1/GRCh38#84367821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333477-A-C

http://identifiers.org/hco/1/GRCh38#84367943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333353-C-A

http://identifiers.org/hco/1/GRCh38#84367954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333344-A-C

84368119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333184-G-A

84368229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333110-T-C

84368232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333107-C-G

84368303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333067-A-G

84368338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146334027-C-T

http://identifiers.org/hco/1/GRCh38#84368428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146333052-C-A

84368428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333052-C-T

84368470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333012-C-T

84368476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146333006-C-G

84368666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332834-C-T

84368726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332775-T-C

84368903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332617-C-T

84368961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332563-G-A

84368961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332563-G-T

84369286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332251-C-G

84369286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332251-C-T

http://identifiers.org/hco/1/GRCh38#84369324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146332216-C-A

84369324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332216-C-T

84369504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146332025-G-A

84369654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146331882-G-C

84369662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146331874-T-C

84369731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146331804-C-T

84370281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146331222-A-G

84370498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146331067-G-T

http://identifiers.org/hco/1/GRCh38#84370550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146331017-C-A

84372361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146330164-T-C

84372363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146330162-T-C

84372370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146330155-A-G

84372537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146330016-T-C

84372552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146330004-C-T

84372693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146329871-A-G

84373889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146328145-C-G

84373899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146328135-T-C

84374098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146327956-A-G

84374146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146327910-C-T

84374207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146327850-G-A

84374269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146327784-G-A

84374386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146327685-C-G

84374715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146327141-C-T

84374926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146326933-T-C

84375097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146326761-G-A

84375121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146326734-T-G

84375763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146326086-G-A

84375809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146326040-T-A

84375939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146325902-T-C

84376361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146324396-A-G

84376458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146324303-C-T

84376584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146324127-A-G

84376702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146324008-T-C

http://identifiers.org/hco/1/GRCh38#84376705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146324005-C-A

84376705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146324005-C-T

84376766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146323939-T-C

84377145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146323593-G-A

84377589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146322864-T-A

84377727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146322740-G-A

84377737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146322730-C-T

84378345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146322150-G-C

84378486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146322031-G-T

84378582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146321013-T-C

84378871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146320758-G-A

84378956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146320670-T-C

http://identifiers.org/hco/1/GRCh38#84378970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146320655-A-C

84379710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146320152-T-C

84379746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146320111-T-C

http://identifiers.org/hco/1/GRCh38#84380010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146319816-A-C

84380023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146319805-A-G

84380166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146319661-A-G

http://identifiers.org/hco/1/GRCh38#84380657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146319264-C-A

84380695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146319227-C-G

84380695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146319227-C-T

http://identifiers.org/hco/1/GRCh38#84381434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146318720-C-A

84381654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146318507-C-T

84381793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146318345-G-A

84381793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146318345-G-C

84381855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146318283-G-T

84382668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146317640-G-A

84382668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146317640-G-C

84382827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146317257-A-G

84384174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146316599-T-C

84384234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146316555-T-C

84384295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146316497-G-T

84384731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146316103-A-G

84384753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 146316081-T-G

http://identifiers.org/hco/1/GRCh38#84384890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146315943-A-C

84384918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146315915-A-T

84384951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146315882-T-A

84385374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146315391-C-T

84385818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146314874-T-A

84385818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146314874-T-C

http://identifiers.org/hco/1/GRCh38#84385879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146314826-C-A

84385880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146314825-T-C

84386016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146314690-G-A

84386016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146314690-G-C

84386256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146314222-G-T

84386612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146313938-C-T

84386633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146313917-G-A

84386633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146313917-G-C

84386756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146313800-C-T

84387036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146313560-C-T

84387524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146313065-G-A

84387549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146312830-G-T

84387673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146312696-G-A

84387816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146312098-A-G

84387940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311988-G-C

84388064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311899-T-A

84388150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311818-G-A

84388181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311783-A-G

84388238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311741-T-C

84388324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 146311657-C-T

http://identifiers.org/hco/1/GRCh38#84388340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146311641-C-A

84388340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 146311641-C-G

http://identifiers.org/hco/1/GRCh38#84388391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146311589-C-A

84388391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 146311589-C-T

http://identifiers.org/hco/1/GRCh38#84388398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146311581-A-C

http://identifiers.org/hco/1/GRCh38#84388430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146311549-C-A

84388440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311539-T-C

84388464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311515-T-C

84388464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146311515-T-G

84389024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146311343-A-G

84389164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146311199-A-T

84389196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146311167-G-T

84389241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 146311124-T-C

http://identifiers.org/hco/1/GRCh38#84389253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#146311112-A-C

84389449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310911-T-C

84389540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310830-A-T

84389581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310789-A-G

84389646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310714-A-T

84389658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310702-A-T

http://identifiers.org/hco/1/GRCh38#84389675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146310686-C-A

84389675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310686-C-T

http://identifiers.org/hco/1/GRCh38#84389684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#146310677-C-A

84389684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 146310677-C-G

84389834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 146310647-G-T

84389932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24582
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 146310543-A-T