16549921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425873-A-G

16549999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425797-T-G

16550008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425788-T-G

http://identifiers.org/hco/2/GRCh38#16550021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12425782-C-A

16550021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425782-C-T

16550063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425753-G-A

16550063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425753-G-C

16550169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425648-A-G

16550206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425617-T-C

16550240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425583-C-T

16550244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425579-A-G

16550652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425216-G-T

http://identifiers.org/hco/2/GRCh38#16550819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12425006-A-C

16550819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12425006-A-G

16550826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424999-G-T

16550866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424965-G-A

16550866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424965-G-T

16550871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424960-G-T

16550990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424841-T-G

16551026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424805-A-G

16551026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424805-A-T

16551320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424537-A-G

16551514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424337-A-G

16551517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424334-T-A

16551517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12424334-T-C

http://identifiers.org/hco/2/GRCh38#16551633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12424236-C-A

16551947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423837-A-G

16551955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423829-T-C

16551956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423828-T-A

http://identifiers.org/hco/2/GRCh38#16552010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12423776-C-A

16552010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423776-C-G

16552010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423776-C-T

http://identifiers.org/hco/2/GRCh38#16552189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12423591-C-A

16552191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423589-G-A

16552195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423585-G-A

16552195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423585-G-T

16552243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423511-G-C

16552355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423403-A-T

16552356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423402-T-C

16552356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423402-T-G

16552427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423331-T-A

16552427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423331-T-C

16552427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423331-T-G

16552443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423312-G-A

16552443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423312-G-T

16552523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423223-A-G

http://identifiers.org/hco/2/GRCh38#16552643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12423100-A-C

16552643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423100-A-G

16552647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423096-T-A

16552647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423096-T-C

16552647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12423096-T-G

16552673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12423070-A-T

16552692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12423051-A-G

16552692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12423051-A-T

16553047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422721-G-A

16553047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422721-G-T

16553052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422716-C-T

16553064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422705-T-A

16553084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422685-T-C

16553084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422685-T-G

16553088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422684-A-G

16553096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422676-T-C

16553107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422665-G-C

16553107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422665-G-T

16553126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422646-A-G

16553188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422459-G-T

16553492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12422200-G-A

16553578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12422119-G-A

16553721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421982-T-C

http://identifiers.org/hco/2/GRCh38#16553817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12421889-C-A

16553828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421861-G-C

16554133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421594-A-G

16554178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421564-T-C

http://identifiers.org/hco/2/GRCh38#16554236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12421503-C-A

16554447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12421314-G-A

16554911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420126-T-A

16554991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420034-T-C

16555001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420028-T-C

16555011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420018-T-C

16555264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12419790-G-T

16555383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12419670-G-T

16555557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12419558-T-C

http://identifiers.org/hco/2/GRCh38#16555715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12418426-C-A

16555722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12418419-T-C

16555790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12418348-A-G

16555884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12418255-A-G

16555891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12418248-T-C

http://identifiers.org/hco/2/GRCh38#16556019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12418131-A-C

16556038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12418112-C-T

16556046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12418104-T-C

16556142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417967-G-A

16556271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417878-T-C

16556317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417832-C-T

http://identifiers.org/hco/2/GRCh38#16556576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12417529-A-C

16556618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417487-C-T

16556829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417286-G-A

16556830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417285-G-A

16557010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417118-G-A

16557022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12417106-C-G

16557189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12416968-T-C

16557377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12416809-C-T

http://identifiers.org/hco/2/GRCh38#16557395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12416793-A-C

16557462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12416751-G-A

16557462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12416751-G-T

16557796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12416110-C-T

16557950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12415958-C-G

16558522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12415646-C-T

16558808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12415361-G-C

http://identifiers.org/hco/2/GRCh38#16558843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12415326-C-A

http://identifiers.org/hco/2/GRCh38#16558849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12415320-A-C

16558903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12415264-G-A

http://identifiers.org/hco/2/GRCh38#16559358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12414958-C-A

16559360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414956-C-T

16559433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414872-G-C

16559442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414863-T-C

16559581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: missense variant
orthologous variants: 12414724-T-C

16559605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414700-C-T

16559645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414667-G-A

16559645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414667-G-T

http://identifiers.org/hco/2/GRCh38#16559683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12414628-C-A

16559719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414584-T-A

16559719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414584-T-C

16559820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414483-T-C

16560126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12414191-G-A

16560591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12412895-A-G

16560645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12412851-A-G

16560645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12412851-A-T

http://identifiers.org/hco/2/GRCh38#16560720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12412783-C-A

16560720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412783-C-T

http://identifiers.org/hco/2/GRCh38#16560766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12412764-C-A

16560766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412764-C-T

16560796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412735-G-T

http://identifiers.org/hco/2/GRCh38#16560818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12412713-C-A

16560818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412713-C-T

http://identifiers.org/hco/2/GRCh38#16560835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12412693-C-A

16560835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412693-C-T

16560838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412690-A-T

http://identifiers.org/hco/2/GRCh38#16560839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12412689-C-A

16560955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412574-G-T

16560964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12412565-A-G

16561114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412414-T-C

16561143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412385-T-C

16561422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412125-A-G

16561441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412106-G-A

16561441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412106-G-C

16561577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12411974-G-C

16561577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12411974-G-T

http://identifiers.org/hco/2/GRCh38#16561639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12411924-C-A

16561639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12411924-C-T

16561654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12411909-G-T

16561862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12411698-C-T

16561943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12411624-A-G

16562087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: missense variant
orthologous variants: 12411488-G-A

16562521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410949-G-C

16562662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410818-C-T

http://identifiers.org/hco/2/GRCh38#16562686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12410796-C-A

16562686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410796-C-T

16562697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410785-A-G

16562922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410568-G-A

16562922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410568-G-T

16563013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410483-A-G

16563021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410475-C-T

16563132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410363-G-A

http://identifiers.org/hco/2/GRCh38#16563203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12410295-A-C

16563515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12410005-A-G

16563862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409448-G-A

16563862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409448-G-T

http://identifiers.org/hco/2/GRCh38#16563878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12409432-A-C

16563878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409432-A-G

16563891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409413-G-A

16563891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409413-G-T

16563905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409399-T-C

16563917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409387-T-C

http://identifiers.org/hco/2/GRCh38#16563920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12409384-C-A

16563953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409351-G-A

16563953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409351-G-T

16564108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409188-G-A

16564108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409188-G-C

16564108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409188-G-T

16564109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409187-T-A

16564109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409187-T-C

16564143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409155-C-T

16564198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409095-G-A

16564198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409095-G-T

16564235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409058-G-A

16564235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409058-G-T

16564236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409057-G-A

16564236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12409057-G-T

16564296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408999-C-G

16564359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408956-T-C

16564419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408902-C-T

16564464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408856-T-C

16564581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408772-G-T

16564766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408607-T-C

16564883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408500-C-T

16564904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408479-T-A

16565066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408342-T-A

16565531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408318-G-A

16565531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408318-G-C

16565531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408318-G-T

http://identifiers.org/hco/2/GRCh38#16565569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12408266-C-A

16565569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408266-C-T

16565575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408260-G-T

16565583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408252-G-C

16565583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408252-G-T

16565589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408246-G-A

16565589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408246-G-T

16565591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408244-G-T

http://identifiers.org/hco/2/GRCh38#16565599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12408236-C-A

16565601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408234-T-C

16565601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408234-T-G

http://identifiers.org/hco/2/GRCh38#16565603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12408232-C-A

16565603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408232-C-T

16565618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408193-T-C

16565631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408180-T-C

16565636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408175-A-G

http://identifiers.org/hco/2/GRCh38#16565650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12408161-C-A

16565650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: missense variant
orthologous variants: 12408161-C-T

16565791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408018-A-G

16565793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12408016-A-G

16565874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12407951-T-C

http://identifiers.org/hco/2/GRCh38#16565987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12407845-A-C

16566192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12407636-C-T

16566200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12407628-C-T

16566221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12407607-A-G

16566248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12407587-G-A

16566542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12406865-T-G

16566552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12406855-G-A

16566922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12406522-A-T

16566926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12406520-T-G

16566995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12406451-C-T

16567801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405854-T-C

16567959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405718-G-A

16568038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405644-T-C

16568067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405579-A-G

16568079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405567-C-G

16568239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405361-A-G

http://identifiers.org/hco/2/GRCh38#16568244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12405356-A-C

http://identifiers.org/hco/2/GRCh38#16568245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12405355-A-C

16568597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12405025-G-A

http://identifiers.org/hco/2/GRCh38#16568832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12404821-C-A

16568832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12404821-C-T

16568887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12404768-G-C

16569196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12404445-G-A

http://identifiers.org/hco/2/GRCh38#16569251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12404395-C-A

16569309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12404337-C-T

16569537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12404119-A-G

http://identifiers.org/hco/2/GRCh38#16569542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12404114-C-A

http://identifiers.org/hco/2/GRCh38#16569685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12403882-A-C

16569696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12403871-A-G

16570521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12402971-C-T

16570758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12402637-G-A

16570758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12402637-G-C

http://identifiers.org/hco/2/GRCh38#16570774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12402616-A-C

16570875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12402506-A-G

http://identifiers.org/hco/2/GRCh38#16571194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12402193-C-A

16571194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12402193-C-T

16571297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12402059-C-G

16571356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12401997-T-C

http://identifiers.org/hco/2/GRCh38#16571499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12401861-C-A

16571499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12401861-C-T

16571727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12401635-A-G

16571920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12401446-G-A

16571948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12401418-A-G

16572025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12401340-T-C

16572479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12400255-C-G

http://identifiers.org/hco/2/GRCh38#16572923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12399641-C-A

http://identifiers.org/hco/2/GRCh38#16573067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12399502-C-A

16573109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12399464-C-T

16573178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12399405-C-G

16583308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12394989-T-C

16583602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12394717-G-C

16583632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12394687-A-G

16583771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12394547-G-A

16584258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12394015-C-G

16584258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12394015-C-T

16584539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393743-T-C

16584597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393685-T-C

16584661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393631-C-T

16584664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393628-C-T

16584707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393578-C-T

16584900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393386-A-T

16584919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393367-T-C

16585009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393291-G-T

16585200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12393122-T-C

16585360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392775-G-T

16585471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392665-C-T

16585479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392659-T-C

16585707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392411-T-C

16585784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392341-G-A

16585828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392329-G-T

16586037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392178-A-G

16586074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392129-G-A

16586079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392124-T-C

16586119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12392084-C-T

16586282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391930-A-G

16586327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391891-T-A

16586327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391891-T-C

16586398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391818-T-C

16586424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391796-C-T

16586562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391652-A-T

16586598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391612-T-C

16586602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391608-G-C

16586643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391596-G-A

http://identifiers.org/hco/2/GRCh38#16586645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12391594-C-A

16586645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391594-C-T

16586882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391382-A-G

16587157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391200-T-C

16587230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12391130-C-T

16588014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12390797-A-T

16588041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12390766-G-A

16588041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12390766-G-T

16588262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12390617-T-A

16588328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12390567-T-C

http://identifiers.org/hco/2/GRCh38#16588441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12390476-A-C

http://identifiers.org/hco/2/GRCh38#16588891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12389514-A-C

16588891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12389514-A-G

16588977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12389425-A-G

16589010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12389395-T-G

16589091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12389313-C-T

16590370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388891-T-A

16590370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388891-T-G

16590442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388823-T-C

16590446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388819-T-C

16590517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388761-T-G

16590607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388671-A-G

16590651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388627-G-A

16590651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388627-G-C

16590651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388627-G-T

16590678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388600-A-T

16590842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388391-T-C

16590899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388331-A-T

16590972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388261-G-A

16590980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388173-A-G

16590995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12388154-G-T

16591333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387826-T-C

16591492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387665-G-C

16591742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387446-A-T

16600492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387248-G-A

16600501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387239-T-C

16600549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387198-A-G

16600564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387183-T-A

http://identifiers.org/hco/2/GRCh38#16600624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12387123-A-C

16600639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387096-T-C

16600660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12387075-T-C

http://identifiers.org/hco/2/GRCh38#16600960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12386794-C-A

16600975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386779-G-A

16601061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386709-T-C

16601208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386570-T-G

16601218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386560-T-C

16601268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386512-T-A

16601324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386474-T-A

16601609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12386276-C-T

http://identifiers.org/hco/2/GRCh38#16601961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12385577-C-A

http://identifiers.org/hco/2/GRCh38#16602540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12384962-A-C

http://identifiers.org/hco/2/GRCh38#16602648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12384852-C-A

16602661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12384839-G-A

16602830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12384692-G-A

16603085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12384406-T-C

16603167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12384291-C-T

http://identifiers.org/hco/2/GRCh38#16603199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12384259-C-A

16603758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12383662-G-C

16604181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12379729-C-T

16604413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12379520-C-T

16604438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12379498-G-A

16604839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377884-G-C

16604946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377787-G-A

http://identifiers.org/hco/2/GRCh38#16605134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12377601-A-C

16605134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377601-A-G

16605265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377374-T-C

16605554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377092-T-A

16605554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377092-T-C

16605572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12377072-G-A

http://identifiers.org/hco/2/GRCh38#16605691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12376951-C-A

16605711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12376931-G-A

16606020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12376667-C-T

http://identifiers.org/hco/2/GRCh38#16606104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12376591-A-C

16606208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12376510-C-T

16606453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12376284-C-T

16606520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12376223-C-T

16607071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12375508-T-C

16607290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12375301-G-A

16607354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12375262-G-C

16607537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12375138-T-A

16608166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12374798-A-G

16608645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12374274-T-G

16608735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12374185-A-G

16608779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12374141-A-G

16608816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12374106-T-C

16608919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12374015-A-G

16608919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12374015-A-T

16609109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12373826-C-T

http://identifiers.org/hco/2/GRCh38#16609189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#12373745-C-A

16609249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12373684-C-G

16609262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12373671-G-A

16609262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12373671-G-T

http://identifiers.org/hco/2/GRCh38#16609275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#12373662-A-C

16609295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12373642-A-G

16609389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12373574-T-C

16609389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12373574-T-G

16609920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12371409-G-T

http://identifiers.org/hco/2/GRCh38#16610274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12371082-C-A

16610364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12370991-T-C

16613587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12368394-G-A

16613685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12368316-G-T

16613753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12368256-C-T

16614236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12367467-G-A

16614259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12367456-T-A

16614279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12367436-C-T

16614342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12367374-A-T

16614353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12367363-A-T

16614421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12367294-T-C

16614447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12367267-T-C

http://identifiers.org/hco/2/GRCh38#16614491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#12367227-C-A

http://identifiers.org/hco/2/GRCh38#16614820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12366643-C-A

16614820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12366643-C-T

16615105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12366216-T-C

16615173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12366146-C-G

16615369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12366013-G-C

16615584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12365816-C-T

16615627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12365756-G-A

16615648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12365735-C-T

16615654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12365729-A-G

16615865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12365349-C-T

16615866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12365348-C-G

16616198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364995-A-G

16616306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364865-T-C

16616406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364756-A-G

16616425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364739-C-T

16616544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364618-G-A

16616564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364584-C-G

16616581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364564-G-T

16616791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364375-C-T

16616983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364199-T-A

16616996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364189-C-T

16617111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364073-A-T

16617114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12364070-T-C

16617212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12364014-A-G

16617325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363918-G-A

16617432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363812-A-T

16618180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363489-A-T

16618333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363334-A-G

16618531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363167-G-A

16618667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363073-G-A

16618685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12363056-G-A

http://identifiers.org/hco/2/GRCh38#16618704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12363037-A-C

16618855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362889-G-T

16618972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362800-G-A

16619009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362774-A-G

16619032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362750-G-A

16619144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362652-G-A

16619153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362643-G-A

16619178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362617-G-A

http://identifiers.org/hco/2/GRCh38#16619185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12362610-C-A

16619216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362579-A-T

16619262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362533-T-A

16619479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12362359-C-T

16619776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12361949-T-C

16620012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12361723-G-A

16620260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12361489-T-C

http://identifiers.org/hco/2/GRCh38#16620313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12361430-A-C

16620590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12361161-C-T

http://identifiers.org/hco/2/GRCh38#16620862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12357693-C-A

16620953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12357613-C-T

16621413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12357178-G-C

16621477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12357115-C-T

16621481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12357111-G-A

16621653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356863-T-C

16621799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356720-T-C

16621875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356645-T-C

16621917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356604-G-A

16621917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356604-G-C

16622150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356366-A-G

16622255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356255-A-G

16622257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356253-T-C

16622415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12356109-T-G

16622683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12355850-G-A

16622737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12355800-T-C

16622749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12355781-C-T

16622832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12355717-T-G

16622845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12355696-T-C

16623118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12355199-C-T

16623123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12355194-T-C

16623131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12355133-A-G

16623384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12354795-A-G

16624068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12354129-C-T

http://identifiers.org/hco/2/GRCh38#16624080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12354117-C-A

16624080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12354117-C-G

16624740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12352990-G-A

16624740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12352990-G-T

16624905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12352817-A-G

16624946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12352421-T-C

http://identifiers.org/hco/2/GRCh38#16625079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12352292-A-C

16625110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12352260-G-A

16625120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12352250-G-T

16625484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12351935-G-A

16625848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12351623-C-T

16626044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12351468-T-C

http://identifiers.org/hco/2/GRCh38#16626122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12351392-A-C

http://identifiers.org/hco/2/GRCh38#16626175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12351279-C-A

16626410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12350839-A-T

16626598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12350635-G-C

16626703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12350552-C-T

16626847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12350433-G-T

16627445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12349938-T-C

16627468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12349921-G-A

16627684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12349656-A-G

16628014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12349313-C-T

http://identifiers.org/hco/2/GRCh38#16628112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12349228-C-A

http://identifiers.org/hco/2/GRCh38#16628348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12348994-C-A

16628379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348963-C-G

16628465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348890-T-C

16628497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348859-T-G

http://identifiers.org/hco/2/GRCh38#16628570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12348783-A-C

16628807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348551-C-T

16629031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348363-G-C

16629051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348343-G-A

16629125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348270-C-T

16629184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348207-C-G

16629245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348148-C-T

http://identifiers.org/hco/2/GRCh38#16629300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12348116-C-A

16629300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12348116-C-T

16629506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12347906-T-C

16629515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12347897-G-A

16630377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12347444-G-A

16630604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12347274-G-C

16630986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346922-G-T

16631027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346872-C-T

16631035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346864-C-T

http://identifiers.org/hco/2/GRCh38#16631047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12346851-C-A

16631193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346720-C-T

http://identifiers.org/hco/2/GRCh38#16631277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12346645-C-A

16631313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346610-G-A

16631339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346583-G-A

16631344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346578-T-C

16631423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346524-T-A

16631443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346522-T-C

http://identifiers.org/hco/2/GRCh38#16631767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12346280-C-A

16631767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346280-C-T

16631781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346266-G-A

16631822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346226-T-C

16631965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12346085-T-C

16632639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345917-G-A

16632878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345709-C-T

16632927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345661-C-T

http://identifiers.org/hco/2/GRCh38#16633026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12345554-A-C

16633183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345411-C-T

16633201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345391-T-C

16633257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345349-G-A

16633900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12345016-A-G

16633934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12344986-G-A

16633960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12344960-A-G

16634371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12344682-T-A

16634371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12344682-T-C

16634875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12344192-A-G

16634967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12343920-G-A

16635243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12343336-C-T

16635278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12343278-G-A

16635341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12343165-T-A

16635341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12343165-T-C

16635475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12343016-C-G

16635525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342970-A-G

16635601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342897-G-A

http://identifiers.org/hco/2/GRCh38#16635889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12342625-C-A

16635889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342625-C-G

16635957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342555-G-A

16635994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342518-G-A

16635994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342518-G-C

http://identifiers.org/hco/2/GRCh38#16636054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12342458-C-A

16636060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342452-C-T

16636104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12342408-A-T

16636592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341899-C-G

16636607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341884-A-T

16637088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341681-T-A

16637135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341637-T-C

16637248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341521-T-G

16637275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341494-T-C

16637463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341313-T-A

16637463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341313-T-C

16637542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341236-C-T

16637590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341185-G-A

16637651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12341143-C-T

16637828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12340972-A-G

16638341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12340485-A-T

16638362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12340453-A-G

16638382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12340434-G-C

16638398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12340418-T-A

16638457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12340347-C-T

16638759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12339987-T-C

16638806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12339950-C-G

http://identifiers.org/hco/2/GRCh38#16638913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12339892-C-A

16639304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12338477-T-C

16639796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12338003-A-G

16639903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12337898-A-G

16639906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12337895-G-C

16640146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12337650-C-T

16640572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12337187-C-T

16640917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12336862-T-C

16640972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12336801-C-T

16640977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12336788-A-G

http://identifiers.org/hco/2/GRCh38#16643959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12335083-C-A

16643959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12335083-C-G

16644459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12334765-C-T

16644616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12334612-T-C

http://identifiers.org/hco/2/GRCh38#16644868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12334368-C-A

16644868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12334368-C-G

16644868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12334368-C-T

16645204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12334043-T-A

16645331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12333916-T-C

16646679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12333602-A-G

16646683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12333598-T-C

16646701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12333580-C-T

16646954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12333348-T-C

http://identifiers.org/hco/2/GRCh38#16647077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12333220-C-A

16647077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12333220-C-G

16647753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12332656-T-C

16647892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12331062-A-G

16648363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12330834-A-T

16648518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12330683-A-G

16648694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12329895-T-C

16648695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12329894-G-A

16649997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12329418-C-T

16650219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12329210-T-G

16650463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12328973-T-C

http://identifiers.org/hco/2/GRCh38#16650709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12328704-A-C

16650855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12328569-G-A

16650914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12328512-T-A

http://identifiers.org/hco/2/GRCh38#16651242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12328198-A-C

16651404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12328011-A-G

16651450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12327967-A-G

16651562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12327857-C-T

16651567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12327852-A-G

16652139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326640-T-C

16652474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326347-T-C

16652559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326261-C-T

16652645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326219-T-C

16652745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326119-C-T

16652777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326087-G-T

16652845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12326027-A-G

16653248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12325519-C-G

16653248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12325519-C-T

16653353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12325432-A-G

16653582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12325001-A-G

16653721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12324868-G-A

16653843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324761-C-T

16653851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324753-A-T

16654001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12324602-G-A

16654005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron_variant, undefined
orthologous variants: 12324597-T-C

16654108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324489-G-A

16654270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324278-A-G

16654388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324173-G-A

16654508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324046-T-A

16654508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12324046-T-C

16654949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323563-T-C

16655035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323461-T-C

16655056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323417-C-T

http://identifiers.org/hco/2/GRCh38#16655185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12323279-A-C

16655188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323276-G-C

16655332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323145-A-G

16655400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323081-G-A

16655420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323061-G-A

16655491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12323009-G-A

16655788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12322743-C-T

16656019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12322504-G-C

16656075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12322437-G-T

16656104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12322410-C-T

16656134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12322380-A-G

16656152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12322371-C-T

16656443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12321629-C-T

16656874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12321032-G-A

16657077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12320875-C-T

16657786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319784-T-C

16657799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319771-G-A

16657965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319613-T-C

16658203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319389-C-T

16658266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319336-G-A

16658279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319323-G-A

16658590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12319027-G-C

16658825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12318740-T-G

16658907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12318662-G-A

16659049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12318532-G-A

16659219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12318395-T-C

16659251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12318362-G-C

16659684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12317884-T-C

http://identifiers.org/hco/2/GRCh38#16659767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12317820-A-C

16660124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12317440-G-T

16660151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12317414-G-A

16660151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12317414-G-T

16660256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12317314-C-G

16660286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12317283-A-T

16660615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12316990-C-T

16661247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12316595-C-T

16661527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12316319-A-T

16661571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12316276-C-T

16661986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12315898-C-T

16662269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12315631-C-T

16662394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12315504-A-T

16662456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12315442-C-T

16662560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12315335-G-C

16662764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12315128-C-T

http://identifiers.org/hco/2/GRCh38#16662860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12315040-C-A

16662995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12314919-A-T

16663204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12314724-C-T

16663340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12314589-T-G

16663509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12314453-G-T

16664242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12313815-C-G

16664242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12313815-C-T

16664729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12313334-T-C

16664842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12313254-T-C

16664855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12313241-G-A

16665419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312632-G-T

16665559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312469-A-G

16665576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312456-G-A

16665683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312348-G-A

16665683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312348-G-T

http://identifiers.org/hco/2/GRCh38#16665798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12312203-C-A

16665798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12312203-C-T

16665814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12312187-G-A

16665814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12312187-G-T

16665834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12312170-T-C

http://identifiers.org/hco/2/GRCh38#16665835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12312169-C-A

16665835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312169-C-T

16665860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312144-C-G

16665860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312144-C-T

16665924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312106-T-C

16665924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312106-T-G

16665926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312104-G-C

16665926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312104-G-T

http://identifiers.org/hco/2/GRCh38#16665964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12312067-C-A

16665964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312067-C-G

16665964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312067-C-T

http://identifiers.org/hco/2/GRCh38#16665975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12312057-C-A

16665975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312057-C-T

16665987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312043-T-A

16665987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12312043-T-C

16666033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12312013-T-C

16666068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12311978-G-A

16666068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12311978-G-T

http://identifiers.org/hco/2/GRCh38#16666180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12311901-C-A

16666180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: intron variant
orthologous variants: 12311901-C-T

http://identifiers.org/hco/2/GRCh38#16666294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12311777-C-A

http://identifiers.org/hco/2/GRCh38#16666320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25373
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#12311753-C-A