17664178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11369377-A-G

17664396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11369213-C-T

17664590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11369015-T-C

17664695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11368923-C-T

17664809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11368807-C-T

17665019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11368571-G-C

17665019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3 prime UTR variant
orthologous variants: 11368571-G-T

17665305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11368035-T-A

17665305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11368035-T-C

17665336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11368028-G-A

17665336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11368028-G-T

17665403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11367967-A-G

http://identifiers.org/hco/2/GRCh38#17665416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11367955-C-A

http://identifiers.org/hco/2/GRCh38#17665429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11367942-C-A

17665429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11367942-C-G

17665429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11367942-C-T

http://identifiers.org/hco/2/GRCh38#17665470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11367905-C-A

17665470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11367905-C-T

http://identifiers.org/hco/2/GRCh38#17665501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#11367881-A-C

http://identifiers.org/hco/2/GRCh38#17665648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11367734-A-C

17666282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11367186-T-A

17666492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11366643-A-G

http://identifiers.org/hco/2/GRCh38#17666528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11366607-A-C

17666550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366585-T-C

17666550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366585-T-G

17666554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366581-G-A

17666554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366581-G-T

17667186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366315-A-G

17667189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366312-G-T

17668725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11366213-G-A

17668990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11365978-C-G

17668991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11365977-C-T

17669169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11365810-G-C

http://identifiers.org/hco/2/GRCh38#17669203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11365776-A-C

17669223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11365760-G-A

17669335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11365639-A-G

17670051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11365051-T-C

http://identifiers.org/hco/2/GRCh38#17670188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11364944-C-A

17670275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364867-G-T

http://identifiers.org/hco/2/GRCh38#17670286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11364856-C-A

17670376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364796-T-A

17670376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364796-T-C

17670382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364790-A-G

17671156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11364125-A-G

17671750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363849-G-T

17671818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363771-T-C

17671850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11363742-T-C

http://identifiers.org/hco/2/GRCh38#17676680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11360801-A-C

17676680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360801-A-G

17676868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360659-T-C

17676984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360565-T-C

17677109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360475-G-C

17677400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360309-T-C

17677514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360208-C-T

17677570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360153-T-C

17677583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360140-T-A

17678051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11359708-C-T

17679011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11359169-T-C

http://identifiers.org/hco/2/GRCh38#17679207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11359036-A-C

http://identifiers.org/hco/2/GRCh38#17679218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11359025-C-A

17679218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11359025-C-T

http://identifiers.org/hco/2/GRCh38#17679232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11359012-C-A

17679252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11358994-G-A

17679252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11358994-G-C

17679335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11358913-G-A

17679335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11358913-G-T

17679392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11358857-T-C

17679414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11358835-A-G

17683004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356827-G-A

17683091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356726-G-A

17683193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356645-G-T

http://identifiers.org/hco/2/GRCh38#17683433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11356415-A-C

17683433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356415-A-G

17683520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356328-G-C

17683547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356303-A-G

17683605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356230-A-G

http://identifiers.org/hco/2/GRCh38#17683734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11356106-A-C

17683786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356054-C-T

17683815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356036-T-A

17683815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356036-T-C

17683836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11356015-A-T

17683956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11355918-T-C

17683956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11355918-T-G

17684136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11355735-A-T

http://identifiers.org/hco/2/GRCh38#17684162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11355708-A-C

17684220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11355664-T-C

17694951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351802-C-G

17694985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351798-G-A

http://identifiers.org/hco/2/GRCh38#17695011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11351773-C-A

17695011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351773-C-G

17695011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351773-C-T

17695119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351698-T-C

17695121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351696-T-C

17695388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351429-T-G

17695426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351294-A-T

17695550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351096-T-A

17695550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351096-T-C

17695613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351053-G-A

17695630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351029-G-C

17695659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11351000-A-G

17695786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11350882-A-G

17695901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11350785-T-C

17700040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11349559-T-C

17700110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11349517-T-C

17700218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11349418-T-C

http://identifiers.org/hco/2/GRCh38#17700442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11349197-C-A

17700504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11349144-T-C

17700724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11348927-T-C

17701197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11348829-T-C

17701705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11348454-G-T

17701875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11348295-T-C

17701911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: splice acceptor variant
orthologous variants: 11348259-T-C

17702165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 11348007-T-C

17702262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11347911-G-A

17702262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11347911-G-C

17702322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11347863-A-G

http://identifiers.org/hco/2/GRCh38#17702802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11347507-A-C

17702932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11347433-G-A

http://identifiers.org/hco/2/GRCh38#17703023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11347394-C-A

17703023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11347394-C-G

17704175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11346795-C-T

17704413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11346575-C-T

17706128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11346333-T-C

17706599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11345760-T-G

17706845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11345498-C-T

http://identifiers.org/hco/2/GRCh38#17706846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11345497-C-A

http://identifiers.org/hco/2/GRCh38#17706949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11345348-C-A

http://identifiers.org/hco/2/GRCh38#17707123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11345170-C-A

17707123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11345170-C-G

17707123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11345170-C-T

17707152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11345146-T-C

17707152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11345146-T-G

http://identifiers.org/hco/2/GRCh38#17707171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11345127-C-A

http://identifiers.org/hco/2/GRCh38#17707219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11345082-C-A

17707255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11345046-G-A

17707255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11345046-G-T

17707257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 11345044-T-C

17707279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11345022-T-A

17707294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11345007-A-G

17707324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11344977-C-G

17707336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11344965-G-A

17707348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11344953-G-A

17707348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11344953-G-T

17707368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 11344933-T-C

http://identifiers.org/hco/2/GRCh38#17707370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11344931-C-A

17707370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11344931-C-G

17707370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 11344931-C-T

17707381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 11344920-T-C

17707406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344898-T-C

17707436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344868-A-G

17707479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344834-T-G

17707501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344812-T-C

17708519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344671-T-A

17708519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344671-T-C

17708519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344671-T-G

17708533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344657-A-G

17708583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344641-T-C

17708597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344626-T-C

17708597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344626-T-G

http://identifiers.org/hco/2/GRCh38#17708634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11344603-C-A

17708634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344603-C-T

17708637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 11344600-A-G

17708831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344422-T-A

17708831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344422-T-C

http://identifiers.org/hco/2/GRCh38#17709053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11344232-C-A

17709053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11344232-C-T

http://identifiers.org/hco/2/GRCh38#17709125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11344161-C-A

17712656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11343792-C-G

17712897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11343583-A-G

http://identifiers.org/hco/2/GRCh38#17713162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11343312-C-A

17713162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11343312-C-T

http://identifiers.org/hco/2/GRCh38#17713359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11343108-C-A

17713359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 11343108-C-T

http://identifiers.org/hco/2/GRCh38#17714884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11341706-A-C

17714884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11341706-A-T

17714984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11341606-C-T

17715122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11341469-C-T

http://identifiers.org/hco/2/GRCh38#17716068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11340908-C-A

17716068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340908-C-T

17716320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340654-T-A

17716320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340654-T-C

http://identifiers.org/hco/2/GRCh38#17716344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11340635-A-C

17716344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340635-A-G

17716574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340227-A-G

17716692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340088-T-A

17716692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11340088-T-C

17716810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11339986-G-A

17716916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339877-A-G

17716936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339856-T-G

http://identifiers.org/hco/2/GRCh38#17716974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11339827-C-A

17716974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339827-C-G

17716974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339827-C-T

17717007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339795-T-A

17717051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339759-T-C

17717051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339759-T-G

17717056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339754-T-C

http://identifiers.org/hco/2/GRCh38#17717438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11339459-A-C

17717438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339459-A-G

17717456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339441-G-A

17718036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339314-T-C

17718041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339309-G-A

17718041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339309-G-C

17718041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339309-G-T

17718053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339297-T-C

17718232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339113-A-G

17718304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339045-A-G

17718304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11339045-A-T

17719483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11338453-C-T

17720006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11337668-C-T

17720178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11336055-T-C

17720185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11336048-T-C

17720268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335971-T-C

17720293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335963-C-T

17720298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335958-C-T

http://identifiers.org/hco/2/GRCh38#17720745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11335582-A-C

17720745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335582-A-T

17720797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335526-A-G

17720806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335517-T-C

17720821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335504-A-G

17720872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335465-A-T

17720894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335448-T-A

17720894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335448-T-C

17720905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335439-A-G

http://identifiers.org/hco/2/GRCh38#17721111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11335241-A-C

17721280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335077-A-G

17721321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11335044-G-T

17724747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11333681-G-A

17724890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11333571-C-T

17724914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11333543-T-C

17725193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11333231-T-C

17725548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11332888-T-C

17726512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11332311-G-T

17726713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11332137-C-T

17731051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330428-A-T

http://identifiers.org/hco/2/GRCh38#17731072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11330407-A-C

17731072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330407-A-T

http://identifiers.org/hco/2/GRCh38#17731166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11330318-C-A

17731166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330318-C-T

17731272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330211-T-A

17731272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330211-T-C

17731369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330121-C-T

17731422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330061-T-C

17731466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11330035-C-T

17731593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329913-T-C

17731598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329908-G-A

17731598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329908-G-T

17731599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329907-T-C

17731600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329906-G-A

17731600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329906-G-T

17731655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329821-T-C

17731655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329821-T-G

http://identifiers.org/hco/2/GRCh38#17731670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11329806-C-A

17731670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329806-C-T

17731703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329773-A-G

17731764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11329717-G-T

17731918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329563-T-C

17731918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329563-T-G

17732128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11329398-T-A

17733114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11328013-A-G

17733472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11327725-A-T

17733488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11327709-T-A

17733488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11327709-T-C

17733779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11327440-G-T

17738705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11325905-T-C

17739021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11325783-G-A

17739181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11325609-G-T

17741050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11324915-T-C

http://identifiers.org/hco/2/GRCh38#17741148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11324823-C-A

17741529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11324183-A-G

17741529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11324183-A-T

17741531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11324181-T-C

17741560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11324152-T-C

http://identifiers.org/hco/2/GRCh38#17741568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11324144-C-A

17741568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11324144-C-G

17741747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11323974-T-C

17741809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11323919-A-G

17741809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11323919-A-T

http://identifiers.org/hco/2/GRCh38#17741825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11323902-C-A

17741994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11323725-G-C

17741994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11323725-G-T

17742403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11323333-T-A

http://identifiers.org/hco/2/GRCh38#17742591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11323017-C-A

17745473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11322203-T-G

http://identifiers.org/hco/2/GRCh38#17745531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11322142-A-C

17745858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: missense variant
orthologous variants: 11321821-C-T

17745982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321697-A-G

17746077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321595-T-A

17746133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321548-G-A

17746133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321548-G-T

17746247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321442-A-G

17746266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321426-G-A

17746313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321400-G-T

17746475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321249-C-T

17746578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11321139-C-T

17748631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11320215-T-C

17748677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11320170-C-T

17748928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11319912-G-A

17748928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11319912-G-T

17749264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11319659-C-G

17751133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11318617-G-A

http://identifiers.org/hco/2/GRCh38#17751530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11318539-A-C

17752834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11316955-T-C

17753041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316753-T-C

17753155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316644-C-T

http://identifiers.org/hco/2/GRCh38#17753169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11316631-C-A

17753407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316442-C-G

17753672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316241-C-T

17753786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316151-C-T

17753790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316140-G-A

17753799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316131-G-A

17753799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11316131-G-T

17753920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315997-G-A

17753941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315976-G-A

17753941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315976-G-T

17753956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315959-G-T

http://identifiers.org/hco/2/GRCh38#17754039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315894-C-A

17754049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315884-T-C

http://identifiers.org/hco/2/GRCh38#17754379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315553-C-A

http://identifiers.org/hco/2/GRCh38#17754532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315520-C-A

17754532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315520-C-T

17754727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315430-T-A

17754727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315430-T-C

17754816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315328-A-G

17754841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315303-T-C

http://identifiers.org/hco/2/GRCh38#17754942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#11315210-C-A

17754942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315210-C-G

17754942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 11315210-C-T

17755150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11315003-G-T

17755249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314898-C-G

17755271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314876-G-A

17755271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314876-G-T

17755321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314843-C-G

17755348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314804-A-G

17755626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11314559-A-G

17755954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314257-G-A

17755980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314228-A-G

17755980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314228-A-T

17756022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314197-T-C

17756184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314080-T-G

17756238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11314037-A-G

17756353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313960-C-T

17758323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313777-G-A

17758323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313777-G-T

17758325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313775-T-A

17758325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 11313775-T-C

17758386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313714-C-G

17758387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313713-T-G

17759162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313170-G-A

17759288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11313053-G-A

17759351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11312990-T-C

http://identifiers.org/hco/2/GRCh38#17759908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11312606-A-C

17759939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 11312571-C-G

17760046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312464-G-A

17760046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312464-G-T

17760061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312449-A-G

17760061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312449-A-T

17760076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312434-A-G

17760076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant
orthologous variants: 11312434-A-T

http://identifiers.org/hco/2/GRCh38#17760123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11312387-C-A

17760123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312387-C-G

17760123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312387-C-T

17760138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312371-A-G

17760138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312371-A-T

http://identifiers.org/hco/2/GRCh38#17760147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11312362-C-A

17760147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312362-C-G

17760147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312362-C-T

17760216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312308-G-A

17760216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11312308-G-T

17761329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron variant
orthologous variants: 11311133-G-A

17761706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310781-A-G

17761708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310779-G-A

17761708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310779-G-T

17761726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310763-G-T

17761925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310573-A-G

17761947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310551-G-A

17761947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310551-G-T

17762338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310012-A-G

17762429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309924-G-A

17762429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309924-G-T

17762491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309759-G-T

17762736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309475-G-A

17763242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308902-T-C

17763287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308859-A-G

17763554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308587-T-C

17763760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308383-C-T

17764103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307933-C-T

17764205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307821-G-A

17764776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307111-G-A

17764776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307111-G-T

17764786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307103-A-T

17764817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307071-A-G

17764829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307059-G-A

17764829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307059-G-T

17764877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307029-C-G

17764877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307029-C-T

17764909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11307001-C-G

17764909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11307001-C-T

17764939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306971-G-C

17764975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306935-A-G

17765008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306902-A-G

17765059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306851-A-G

17765122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306783-T-C

17765123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11306782-T-A

http://identifiers.org/hco/2/GRCh38#17766502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11305329-C-A

17766502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305329-C-T

17766747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305111-T-A

17766764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305093-T-C

17766810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305026-A-G

17766910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304845-G-A

17766912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304843-A-T

17767066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11304705-T-C

17768724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304437-C-T

http://identifiers.org/hco/2/GRCh38#17768821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11304340-A-C

17768821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304340-A-G

17768821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304340-A-T

17768841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304321-T-C

http://identifiers.org/hco/2/GRCh38#17768847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11304315-C-A

17769218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304036-T-C

17769219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304035-A-G

17769944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303462-A-G

http://identifiers.org/hco/2/GRCh38#17770110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11303306-A-C

17770360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303066-T-C

17770420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303008-A-G

17770888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302334-G-A

17770954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302307-T-C

17770975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302286-A-G

http://identifiers.org/hco/2/GRCh38#17771020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11302247-C-A

17771029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11302238-A-T

17771236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11302051-C-T

17771278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11302012-T-C

17771292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301998-G-A

17771414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11301913-T-C

17772142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11301296-G-T

17772150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11301288-G-T

17772293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301155-C-T

17772388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301081-C-G

17772469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301011-G-A

17772525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300969-T-G

17772553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300942-T-C

17772593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300903-A-G

17772608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300888-T-G

17772635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 11300862-T-G

17772708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11300789-G-A

http://identifiers.org/hco/2/GRCh38#17772753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300744-C-A

17772753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11300744-C-T

http://identifiers.org/hco/2/GRCh38#17772759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300738-A-C

http://identifiers.org/hco/2/GRCh38#17772805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300694-A-C

17772805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300694-A-G

http://identifiers.org/hco/2/GRCh38#17772973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11300207-C-A

17772973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300207-C-G

17772987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300188-A-G

17773026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300151-T-A

17773026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300151-T-G

17773033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300144-G-A

17773261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11299167-G-T

17773305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299123-T-C

http://identifiers.org/hco/2/GRCh38#17773509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11298909-A-C

17773514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298904-T-C

17773805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298715-C-T

17773976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298628-G-C

17774073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298538-G-A

17774204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298412-T-A

17774204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298412-T-C

17774204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298412-T-G

17774239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298376-A-G

17774292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11298323-G-A

17774292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11298323-G-T

17774337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11298278-A-G

17777466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11297092-A-G

17777565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11297005-A-G

17777577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296993-C-T

17777604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296966-G-C

17777871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296472-G-A

17777901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296442-T-C

17777963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296388-T-C

17777963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296388-T-G

17778078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296273-T-C

17778080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296271-A-G

http://identifiers.org/hco/2/GRCh38#17778118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11296234-C-A

17778544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296152-T-C

17778580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296119-A-G

17778670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296035-T-G

http://identifiers.org/hco/2/GRCh38#17778691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11296014-C-A

17780008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11293302-G-A

17780015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11293295-T-C

17780125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293185-A-G

17780131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293179-G-A

17780131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293179-G-T

http://identifiers.org/hco/2/GRCh38#17780153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11293166-A-C

17780153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293166-A-G

17780163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293158-G-A

17780163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293158-G-T

http://identifiers.org/hco/2/GRCh38#17780175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11293146-C-A

17780175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293146-C-T

17780239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293096-A-G

17780244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293092-T-C

http://identifiers.org/hco/2/GRCh38#17780269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11293067-C-A

17780269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11293067-C-T

17780382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292848-T-G

17780607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292589-T-C

17780742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292448-G-A

17780742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292448-G-T

17780884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292306-G-T

17780894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292296-A-G

17780959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292231-C-T

17780983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11292207-G-T

17781134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292074-C-G

17781172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292039-A-T

17781191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11292020-T-G

17781207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11292004-T-G

17781213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291998-A-G

17781264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291947-T-C

17781290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291921-T-A

17781290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291921-T-C

http://identifiers.org/hco/2/GRCh38#17781291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11291920-C-A

17781291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291920-C-T

17781362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291852-C-T

17781423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291791-T-C

17781454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291766-T-C

17781455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291765-A-G

17781459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11291761-A-G

http://identifiers.org/hco/2/GRCh38#17781470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11291750-C-A

17781470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291750-C-G

17781470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291750-C-T

17781575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291639-A-G

17781647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291567-A-G

17781655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291559-T-C

http://identifiers.org/hco/2/GRCh38#17781854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11291360-A-C

17781854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291360-A-G

17781854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11291360-A-T

17781902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11291312-T-G

17781979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11291234-T-C

17781983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11291230-A-G

17781983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11291230-A-T

17782117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290980-A-G

17782118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290979-A-G

17782157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290939-T-C

17782695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290340-G-A

17782719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290313-C-T

17782864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11290157-G-A

17784532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11287047-T-C

http://identifiers.org/hco/2/GRCh38#17784560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11287019-C-A

17784560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11287019-C-T

17784635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286945-A-G

17784635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286945-A-T

17784801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286782-C-T

17785278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286428-T-C

17785345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286367-G-T

17785478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286249-T-A

http://identifiers.org/hco/2/GRCh38#17785507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11286218-C-A

17785508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286217-A-G

17785564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286162-T-C

17786056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11286041-A-G

17786201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285887-G-T

17786241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285856-A-G

17786241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285856-A-T

17786277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285823-C-T

17786319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285778-A-G

17786379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285725-A-G

17786394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285710-A-G

17786411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11285689-G-T

17786735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283548-T-C

17786857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283439-G-A

17786857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283439-G-T

http://identifiers.org/hco/2/GRCh38#17786875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283423-C-A

17786909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283394-T-C

17786944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283364-A-G

17786944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283364-A-T

http://identifiers.org/hco/2/GRCh38#17786971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283337-C-A

17786971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283337-C-T

http://identifiers.org/hco/2/GRCh38#17786974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283334-C-A

17786974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283334-C-T

http://identifiers.org/hco/2/GRCh38#17786998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283321-C-A

17787076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283235-T-C

17787091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283222-T-C

http://identifiers.org/hco/2/GRCh38#17787160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283172-C-A

17787160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283172-C-T

17787167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283168-A-T

http://identifiers.org/hco/2/GRCh38#17787369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11283053-C-A

17787372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11283050-C-T

http://identifiers.org/hco/2/GRCh38#17787518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11282917-C-A

17787765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282845-A-G

17787959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282807-T-C

17787967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282795-G-T

17788029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282738-T-C

17788081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282678-C-T

17788178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282592-T-A

17788356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282403-T-G

http://identifiers.org/hco/2/GRCh38#17788612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11282168-C-A

17788663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282055-T-A

17788667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11282051-G-C

17788902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11281902-A-T

17789066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281754-G-C

17789066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281754-G-T

17789436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281378-G-A

17790765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11280758-A-G

17790839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11280610-A-G

17790859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11280588-A-G

17790871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11280576-T-C

17791241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11280033-G-A

17791515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279782-G-A

17791716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279603-G-T

17791838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279090-T-C

17791890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279054-G-A

17792058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278894-T-C

17792093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278856-G-C

17792116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278833-G-C

17792376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278564-C-T

17792512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278417-T-C

17792513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278416-G-A

http://identifiers.org/hco/2/GRCh38#17792823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11277722-C-A

17792823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11277722-C-G

17792823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11277722-C-T

http://identifiers.org/hco/2/GRCh38#17793001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11277542-C-A

http://identifiers.org/hco/2/GRCh38#17793228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11277334-C-A

17793233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11277329-T-G

17793283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11277283-G-A

http://identifiers.org/hco/2/GRCh38#17794065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11276545-C-A

17794233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276382-C-T

17794388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276209-C-T

17794403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276194-C-T

17794502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276102-G-T

17794739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275864-G-A

17794772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275836-A-G

17794791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275806-G-A

17794791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275806-G-T

http://identifiers.org/hco/2/GRCh38#17794794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11275803-C-A

17795824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275171-T-C

17795869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275120-C-G

17796062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274924-G-T

17796108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274897-T-C

17796123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274884-C-G

17796130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274877-A-G

17796142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274862-T-C

17796336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274719-A-G

17798222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273622-G-A

17798424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273456-T-C

17798508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273378-T-C

17798596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273290-T-C

17798735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273178-A-G

http://identifiers.org/hco/2/GRCh38#17798869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11273077-C-A

17798869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273077-C-T

17798873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273073-C-T

17798976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272970-T-C

17799070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272890-A-G

17799074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272886-T-A

http://identifiers.org/hco/2/GRCh38#17799274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#11272721-C-A

17799274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272721-C-G

17799278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272716-G-A

17799729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11272185-A-G

17799735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11272179-G-T

17799961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272017-T-C

17800084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271890-A-G

17800104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20466
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 11271879-C-T