205228003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: 132319435-G-A

205228036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: 132319405-C-T

http://identifiers.org/hco/1/GRCh38#205228179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132319288-C-A

205228179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: 132319288-C-G

205228179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: 132319288-C-T

http://identifiers.org/hco/1/GRCh38#205228207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132319260-A-C

205228259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: 132319209-G-A

205228259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: 132319209-G-T

http://identifiers.org/hco/1/GRCh38#205228313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132319159-C-A

http://identifiers.org/hco/1/GRCh38#205228874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132318613-C-A

205228874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron variant
orthologous variants: 132318613-C-T

205228954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132318537-G-A

205228954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132318537-G-T

205229044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132318449-G-A

205229044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132318449-G-C

205229049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 132318443-A-G

http://identifiers.org/hco/1/GRCh38#205229503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132318260-C-A

205229503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron variant
orthologous variants: 132318260-C-T

http://identifiers.org/hco/1/GRCh38#205229845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132317951-C-A

http://identifiers.org/hco/1/GRCh38#205229904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132317892-C-A

205229904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132317892-C-T

205229958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132317838-A-G

205229962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132317834-A-T

205230050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132317747-T-C

http://identifiers.org/hco/1/GRCh38#205230069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132317732-C-A

205230069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132317732-C-T

205230091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132317709-A-G

205230175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132317632-T-C

http://identifiers.org/hco/1/GRCh38#205230287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132317522-C-A

205230287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317522-C-T

205230997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317112-T-A

205230997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317112-T-C

205230997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317112-T-G

205230999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317110-C-G

205231015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317094-G-A

205231015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317094-G-C

http://identifiers.org/hco/1/GRCh38#205231093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132317043-A-C

205231093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132317043-A-G

205231737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132316751-G-A

205232184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132316223-A-G

205232272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132316125-G-A

205232330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132316065-T-G

205232419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132316002-A-T

205232428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315993-T-C

205232444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315977-G-T

205233190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315675-G-C

205233307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315599-G-C

205233485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315439-G-A

205233516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315424-C-T

205233539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315402-T-G

205233550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315391-G-A

205233590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315359-A-G

205233665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315263-T-C

205233717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315210-G-A

http://identifiers.org/hco/1/GRCh38#205233763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132315173-C-A

205233763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315173-C-G

205233763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132315173-C-T

205233832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132315065-G-C

205233832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132315065-G-T

205233939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132314886-T-C

205233962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132314856-A-G

205233973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132314845-T-A

205233975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132314843-C-T

http://identifiers.org/hco/1/GRCh38#205234100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132314758-C-A

205234100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132314758-C-T

205235099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132314378-G-C

205236196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132313660-T-A

205236591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132313332-G-T

205236649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132313277-T-A

205236672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132313254-G-A

205236840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132313107-G-A

http://identifiers.org/hco/1/GRCh38#205236842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132313105-C-A

http://identifiers.org/hco/1/GRCh38#205236950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132312993-C-A

205237154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132312786-T-C

205237186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132312754-G-A

205237215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132312714-C-T

205237422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132312504-G-A

205237832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132312105-G-T

205237945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311999-C-T

205238013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132311943-A-G

205238259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132311676-T-C

205238461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311535-A-G

205238472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311524-C-T

205238473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311523-G-A

205238473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311523-G-C

205238597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311414-G-A

http://identifiers.org/hco/1/GRCh38#205238695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#132311316-C-A

205238706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132311313-T-C

205239164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310872-G-C

205239164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310872-G-T

205239248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310799-G-A

205239286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310760-G-A

205239298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310748-C-T

205239646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310397-T-A

205239646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310397-T-G

205239702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310355-G-A

205239979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132310149-A-G

http://identifiers.org/hco/1/GRCh38#205240030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132310078-A-C

http://identifiers.org/hco/1/GRCh38#205240033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132310075-C-A

205240301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132309830-A-G

205240340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132309789-C-T

205241443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132308980-C-T

205241491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132308932-C-T

205241498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132308924-C-G

205241498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132308924-C-T

205241700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132308722-G-A

205241772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132308650-C-T

205241788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132308634-G-A

205241961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132308476-T-C

205242135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132308337-C-T

205242227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132308251-T-G

205242731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132307823-A-G

205242959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132307657-T-G

205244852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132306926-G-A

205244974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132306621-A-G

205245108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132306477-A-G

205245308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132306322-A-G

205245502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132306196-T-A

205245633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132306099-T-C

205246123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304929-G-T

205246167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304884-A-G

205246189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304861-G-A

205246263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304798-G-T

http://identifiers.org/hco/1/GRCh38#205246714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132304381-A-C

205246714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304381-A-G

205246811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304296-G-A

205246811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304296-G-T

http://identifiers.org/hco/1/GRCh38#205246814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132304293-C-A

http://identifiers.org/hco/1/GRCh38#205246829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132304280-C-A

205246833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304276-A-G

205246847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132304260-G-A

205248116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132302919-A-G

205248809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132302556-A-G

205248978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132302366-C-T

205250082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132301348-G-A

http://identifiers.org/hco/1/GRCh38#205250423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132301122-C-A

205250423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132301122-C-T

205250980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132300790-A-T

205251061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132300713-C-G

205251130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132300646-C-T

205251736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132300084-A-G

205251843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132300004-G-A

205252091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299755-A-G

205252317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299540-G-A

205252396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299432-C-T

205252410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299418-G-A

205252487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299335-G-C

205252604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299261-G-A

205252604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299261-G-C

205252771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299137-T-A

http://identifiers.org/hco/1/GRCh38#205252785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132299123-A-C

205252785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299123-A-G

205252797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299111-G-A

205253016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299070-C-T

205253075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132299032-C-G

205253146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298968-G-A

205253356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298822-G-A

205253518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298672-A-G

205253519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298671-T-C

205253522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298668-A-G

205253835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298367-T-C

205253851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298351-T-C

205253880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298322-A-G

205253965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298274-A-G

205254064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298196-A-T

205254080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132298189-G-T

205254523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132297818-C-G

205254704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132297665-G-A

205254833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132297507-C-G

205255574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132296216-G-A

205255574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132296216-G-T

205255669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132296128-A-G

205255706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132296093-G-A

205255710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132296089-A-G

205256102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132295725-G-A

205256102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132295725-G-T

http://identifiers.org/hco/1/GRCh38#205256111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#132295713-C-A

205256111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132295713-C-G

205256111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132295713-C-T

205256186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132295638-T-G

http://identifiers.org/hco/1/GRCh38#205256311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132295536-C-A

205256311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132295536-C-T

205256475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132295363-A-G

205256511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132295329-G-T

205256537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132295305-G-T

http://identifiers.org/hco/1/GRCh38#205256725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132295155-C-A

205257063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294941-T-A

http://identifiers.org/hco/1/GRCh38#205257192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132294819-C-A

205257192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132294819-C-T

205257196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132294811-A-G

205257204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132294803-G-A

205257205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132294802-A-G

205257223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132294784-G-A

205257248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132294735-G-A

205257248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132294735-G-T

205257388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294582-A-G

205257427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294539-G-A

205257427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294539-G-T

205257454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294512-G-A

205257454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294512-G-C

205257454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294512-G-T

205257483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294509-A-G

205257483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294509-A-T

205257771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294324-G-A

205257891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294230-G-T

205258063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294062-G-T

205258095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294030-G-A

205258174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132294003-G-A

205258398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132293808-G-T

205258493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132293736-A-G

205258977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132293138-C-T

205259753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132292825-G-A

205260527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132292156-T-G

205260855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132291914-C-T

205260873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132291895-G-A

http://identifiers.org/hco/1/GRCh38#205261232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132291543-A-C

205261232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132291543-A-G

205261232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132291543-A-T

205261378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132291407-A-T

205266710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132290459-A-G

205266909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132290298-G-A

205267237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132290061-G-A

205267285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132290013-G-A

205267406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132289918-T-C

205267412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132289912-C-G

205267567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132289831-T-C

205267754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289711-C-T

205267774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289692-T-A

http://identifiers.org/hco/1/GRCh38#205267787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132289679-C-A

205267802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289664-G-A

http://identifiers.org/hco/1/GRCh38#205267833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132289633-C-A

205267833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289633-C-T

205267896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289594-C-G

205268039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289454-A-G

205268791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289132-G-A

205268791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289132-G-T

205268796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289125-A-G

205268861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289051-A-G

205268861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132289051-A-T

205269037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288858-G-T

205269229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288666-T-C

205269334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288561-C-T

205269364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288531-G-A

http://identifiers.org/hco/1/GRCh38#205269385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132288510-A-C

205269385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288510-A-G

205269403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288492-G-A

205269460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288435-G-A

205269460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288435-G-T

205269533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132288362-A-G

http://identifiers.org/hco/1/GRCh38#205269911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132287978-A-C

205269911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287978-A-G

205269911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287978-A-T

205269973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287916-G-A

205269973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287916-G-C

205269973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287916-G-T

205270043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287842-T-C

http://identifiers.org/hco/1/GRCh38#205270233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132287681-C-A

205270233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287681-C-G

205270233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287681-C-T

205270283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287644-A-G

205270506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287323-G-A

http://identifiers.org/hco/1/GRCh38#205270521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132287311-C-A

205270521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287311-C-T

205270562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287276-C-G

205270676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287177-C-T

205270802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132287054-C-T

205270970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132286909-T-G

205270997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132286887-A-G

205271024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286861-G-T

205271026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286857-G-A

205271026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286857-G-T

http://identifiers.org/hco/1/GRCh38#205271315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#132286564-A-C

205271341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286522-C-T

205271342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286521-A-G

205271448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286420-A-G

205271465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132286403-G-T

205271704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132286203-T-C

205271912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132285454-C-T

205271984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132285382-A-G

205271996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132285370-A-G

205272295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132285084-T-C

205272309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132285070-G-A

205272309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132285070-G-T

http://identifiers.org/hco/1/GRCh38#205272347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132285032-C-A

205272347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132285032-C-T

205272382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284995-G-A

205272382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284995-G-T

205272423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284954-A-G

205272423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284954-A-T

http://identifiers.org/hco/1/GRCh38#205272429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132284948-C-A

205272429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284948-C-T

205272535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284852-T-A

205272535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284852-T-C

205272535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132284852-T-G

http://identifiers.org/hco/1/GRCh38#205272641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132284766-C-A

205272641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284766-C-T

205272757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284663-G-A

205272757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284663-G-T

205272774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284639-T-C

http://identifiers.org/hco/1/GRCh38#205272903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132284506-C-A

205272903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284506-C-G

205272954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284453-A-G

http://identifiers.org/hco/1/GRCh38#205272973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132284434-C-A

205273068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284326-G-T

205273101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284293-T-C

205273111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284279-G-A

205273111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132284279-G-T

205273351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132284043-T-C

http://identifiers.org/hco/1/GRCh38#205273446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#132283963-C-A

205273678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132283719-G-A

205273711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132283690-A-G

205273726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132283675-G-A

205274053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132283372-T-A

205274094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132283325-G-A

205274204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132283240-G-A

205274492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132282951-G-A

205274615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132282847-C-G

205275112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132282637-T-C

205275333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132282454-C-T

205275700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132282176-C-G

205275700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132282176-C-T

205276198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132281770-T-C

205276290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132281693-G-A

http://identifiers.org/hco/1/GRCh38#205276743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132281253-C-A

205277894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132280976-C-G

205278527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132280471-A-G

205283647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132275172-C-T

205284104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132274735-C-T

http://identifiers.org/hco/1/GRCh38#205284381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#132274523-C-A

205284381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132274523-C-T

205284835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132274099-G-A

205284955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132273985-A-G

205285024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24239
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132273906-G-A