http://identifiers.org/hco/3/GRCh38#183178927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19537136-C-A

183179026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3 prime UTR variant
orthologous variants: 19537227-G-T

http://identifiers.org/hco/3/GRCh38#183179455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19537589-C-A

183179455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 19537589-C-T

http://identifiers.org/hco/3/GRCh38#183179459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19537600-C-A

183179459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 19537600-C-T

http://identifiers.org/hco/3/GRCh38#183179479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19537620-C-A

183179479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 19537620-C-T

183179481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19537622-C-G

183179501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 19537639-G-A

183179501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 19537639-G-T

183179535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19537673-G-A

183179535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19537673-G-C

183179535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19537673-G-T

183179557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19537698-C-G

183179557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19537698-C-T

183179564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 19537709-C-T

183179569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 19537714-A-T

183179640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19537780-G-T

183179875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19537991-C-T

183179947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19538027-C-G

http://identifiers.org/hco/3/GRCh38#183179952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19538032-C-A

183180122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19538178-A-G

183180135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19538191-G-T

183180223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19538282-G-A

http://identifiers.org/hco/3/GRCh38#183180234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19538293-C-A

183180235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19538294-A-G

183180246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19538304-G-A

183180246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19538304-G-T

http://identifiers.org/hco/3/GRCh38#183180263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19538322-C-A

183180263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19538322-C-G

183180263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19538322-C-T

183181633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19539860-T-C

183181727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19539931-A-G

183182069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19540162-C-T

183182092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19540184-G-A

183182222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19540293-G-C

183182411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19540462-G-T

183182486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19540541-G-T

183182539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540594-T-C

183182541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540596-T-C

183182545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540608-G-A

183182545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540608-G-T

http://identifiers.org/hco/3/GRCh38#183182546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19540609-C-A

183182546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540609-C-T

183182559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540622-T-A

183182559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540622-T-C

183182559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540622-T-G

183182593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540662-G-A

183182593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540662-G-T

183182647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540689-G-A

183182652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 19540694-T-C

183182693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 19540718-C-T

http://identifiers.org/hco/3/GRCh38#183182729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19540752-C-A

183182729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540752-C-T

http://identifiers.org/hco/3/GRCh38#183182738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19540761-C-A

183182740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540763-C-T

183182766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540787-A-G

http://identifiers.org/hco/3/GRCh38#183182768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19540789-C-A

http://identifiers.org/hco/3/GRCh38#183182788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19540809-C-A

183182844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540862-C-T

183182887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19540907-G-A

183183501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541141-A-G

183183509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541148-T-C

183183779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541397-A-G

183183784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541402-G-T

183184343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541708-T-C

183184343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541708-T-G

183184407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541764-C-G

183184497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19541849-T-C

183185363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19543581-G-T

183248086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19570426-G-A

183249171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575523-A-T

183249182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575534-A-G

183249194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19575551-A-G

183249219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19575576-A-G

183249277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19575630-G-C

183249431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19575821-G-A

183249431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19575821-G-C

http://identifiers.org/hco/3/GRCh38#183249527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19575908-A-C

183249662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576032-G-A

183250085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576326-T-A

183250156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19576383-G-A

http://identifiers.org/hco/3/GRCh38#183250681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19576544-C-A

183251578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19577402-T-A

183251760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19577518-G-A

183252770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578586-T-G

183252866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578705-T-C

183252938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578766-C-G

183253110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578903-T-C

http://identifiers.org/hco/3/GRCh38#183253131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19578924-C-A

183253143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578932-G-A

183253143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578932-G-C

183253143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578932-G-T

183253161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578944-G-A

183253161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578944-G-T

183253180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19578963-C-T

http://identifiers.org/hco/3/GRCh38#183253214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579003-A-C

183253214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579003-A-G

183253260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579076-G-A

183253260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579076-G-C

http://identifiers.org/hco/3/GRCh38#183253295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579109-C-A

http://identifiers.org/hco/3/GRCh38#183253437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579238-C-A

183253437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19579238-C-T

183253468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19579261-T-C

183253468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19579261-T-G

183253671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579454-G-T

http://identifiers.org/hco/3/GRCh38#183253684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579467-C-A

183253766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19579551-C-T

183253863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579605-G-A

183253863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579605-G-C

183253863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579605-G-T

http://identifiers.org/hco/3/GRCh38#183253887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579630-C-A

183253887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579630-C-G

183253887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579630-C-T

183253903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579646-G-T

183253911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579654-C-T

183254026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579756-C-T

183254071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19579779-G-A

183254071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19579779-G-T

183254116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579799-C-T

183254148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19579811-G-A

http://identifiers.org/hco/3/GRCh38#183254335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579881-C-A

183254335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579881-C-T

183254345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579891-G-A

183254345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579891-G-T

183254364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579907-G-T

http://identifiers.org/hco/3/GRCh38#183254378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19579921-C-A

183254378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19579921-C-T

183254466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19580005-G-A

183254466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19580005-G-C

183254529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580075-C-G

183254529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580075-C-T

183254713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19580196-A-G

183254746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19580227-A-G

183254792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19580279-A-G

http://identifiers.org/hco/3/GRCh38#183255464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19580980-C-A

183255464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19580980-C-T

183255717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581229-G-T

183255790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581317-T-C

183255841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581344-A-T

183256100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19581596-T-C

183257080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19583607-C-T

183257138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19583658-C-T

183257383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19583913-A-G

183257634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19584130-C-T

http://identifiers.org/hco/3/GRCh38#183257681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19584173-C-A

183264458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19584386-T-C

183264871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19584837-C-T

183266630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585694-G-C

183266676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585740-A-G

183266744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585808-G-T

183266745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19585809-G-C

183268316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586666-G-C

183268320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586668-A-G

183268422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19586751-G-C

183269501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587503-G-A

183269501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587503-G-T

183269533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587542-G-T

http://identifiers.org/hco/3/GRCh38#183269592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19587601-C-A

183269610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587617-T-C

183269612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587619-C-T

http://identifiers.org/hco/3/GRCh38#183269651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19587659-C-A

183269651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587659-C-T

183269653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587661-A-G

183269706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587715-G-T

183269707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19587716-A-T

183269913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19587891-A-G

183269913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19587891-A-T

183269996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19587974-C-T

183270004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19587982-C-T

183270189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19588167-T-G

183270236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19588214-G-A

183270241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 19588219-G-A

183270789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19588767-G-C

183270917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19588895-T-C

http://identifiers.org/hco/3/GRCh38#183270941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19588919-C-A

183270941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19588919-C-T

183270956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19588935-T-C

http://identifiers.org/hco/3/GRCh38#183270962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19588941-C-A

183270962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19588941-C-T

http://identifiers.org/hco/3/GRCh38#183271013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19588996-C-A

183271013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19588996-C-G

183271013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19588996-C-T

183271151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589113-A-G

183271222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589180-G-A

http://identifiers.org/hco/3/GRCh38#183271280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19589237-C-A

183271280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589237-C-T

183271318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589275-T-A

183271338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589294-G-T

183271365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589320-T-A

183271386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589342-G-A

183271761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589694-T-C

http://identifiers.org/hco/3/GRCh38#183271901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19589870-C-A

183271964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589926-A-G

http://identifiers.org/hco/3/GRCh38#183271966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19589927-C-A

183271966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589927-C-T

183272022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19589979-T-C

183272060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590019-G-T

183272169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590121-T-C

183272177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590127-A-G

183272189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590137-T-C

183272304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590252-T-C

183272311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590259-G-A

183272311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590259-G-C

183272311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590259-G-T

183272322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590269-G-A

http://identifiers.org/hco/3/GRCh38#183272398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19590341-C-A

183272418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590359-G-A

http://identifiers.org/hco/3/GRCh38#183272786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19590713-C-A

183272786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590713-C-T

http://identifiers.org/hco/3/GRCh38#183272822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19590753-C-A

183272822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590753-C-T

http://identifiers.org/hco/3/GRCh38#183272891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19590822-A-C

183272946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590881-A-G

183272996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590922-T-C

183273160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590984-G-A

183273160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19590984-G-T

183273200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19591027-A-G

http://identifiers.org/hco/3/GRCh38#183273305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19591133-C-A

183274722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19591686-T-C

183274724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19591688-T-C

183275347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19593105-T-A

183275467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19593215-T-G

183275529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19593266-G-A

183275966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19593362-A-T

183275969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19593365-A-G

183275969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19593365-A-T

183276616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19598259-T-G

http://identifiers.org/hco/3/GRCh38#183276617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19598260-C-A

http://identifiers.org/hco/3/GRCh38#183276626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19598269-C-A

183276626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19598269-C-T

183276712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598352-A-G

183276799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598439-G-A

183276799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598439-G-T

183276801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598441-A-G

183276878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598484-G-A

183276878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598484-G-T

183276906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 19598508-G-A

183276906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598508-G-T

183276933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598537-G-A

183276933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19598537-G-C

183277022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19598613-T-G

183277035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19598630-G-A

183277035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19598630-G-T

183298384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604805-A-G

183298406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19604825-G-A

183298878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605234-C-T

183298894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605250-G-A

183298897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605253-C-G

183299009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605369-G-T

183299022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605382-G-A

183299022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605382-G-T

183299092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605431-G-A

183299116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605455-G-C

183299116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605455-G-T

183299120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605459-C-T

183299316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605540-A-T

183299345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605567-G-T

http://identifiers.org/hco/3/GRCh38#183299475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19605697-C-A

183299475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605697-C-T

183299516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19605736-G-A

http://identifiers.org/hco/3/GRCh38#183299690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19605890-C-A

183309506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19609014-G-A

183309591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19609092-G-A

183309591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19609092-G-T

http://identifiers.org/hco/3/GRCh38#183309684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19609167-C-A

http://identifiers.org/hco/3/GRCh38#183309687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19609170-C-A

183309692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19609174-A-G

183312409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19616832-G-A

183312515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19616927-T-C

183321912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623010-C-T

183322866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623664-G-A

183322866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623664-G-C

183323126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623863-G-A

183323126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623863-G-C

183323126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623863-G-T

183323153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623892-G-A

183323153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623892-G-C

183323153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19623892-G-T

http://identifiers.org/hco/3/GRCh38#183323194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19624002-C-A

183323194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624002-C-G

183323194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624002-C-T

http://identifiers.org/hco/3/GRCh38#183323196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19624004-A-C

183323196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624004-A-G

183323198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624006-G-A

183323198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624006-G-T

183323200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624008-G-A

183323200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624008-G-C

183323202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624010-G-A

183323202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624010-G-C

183323202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624010-G-T

http://identifiers.org/hco/3/GRCh38#183323204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19624012-C-A

183323204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624012-C-G

183323204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624012-C-T

183323206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624014-G-A

http://identifiers.org/hco/3/GRCh38#183323239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19624072-C-A

183323239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19624072-C-T

183323410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624247-T-C

183323820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624292-T-C

183324175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19624635-C-G

183330645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632748-C-T

183330650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632752-G-A

183330697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632810-C-T

183330781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19632903-C-G

183351486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19639344-T-C

183351642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19639465-G-T

183351804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19639746-A-G

183351806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19639776-A-G

183352068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19643385-G-A

183375518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19661533-C-T

http://identifiers.org/hco/3/GRCh38#183375652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19661641-C-A

183375652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19661641-C-T

183375921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19661898-A-G

http://identifiers.org/hco/3/GRCh38#183375932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19661911-C-A

http://identifiers.org/hco/3/GRCh38#183375992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19661973-C-A

183375992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19661973-C-G

183376024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19661997-G-C

183376024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19661997-G-T

http://identifiers.org/hco/3/GRCh38#183376074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19662039-C-A

183376074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19662039-C-T

http://identifiers.org/hco/3/GRCh38#183377574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19662735-C-A

183377574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19662735-C-G

183377745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19662891-T-G

183377836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19662978-T-C

183377857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19662996-A-G

183377885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663036-G-A

183377885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663036-G-T

183377913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663066-A-G

183378174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663297-G-A

183378174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663297-G-T

183378283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663400-A-G

183378283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663400-A-T

183378352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663469-C-T

http://identifiers.org/hco/3/GRCh38#183378355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19663472-C-A

183378365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663482-G-A

183378365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663482-G-T

http://identifiers.org/hco/3/GRCh38#183378407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19663505-C-A

183378410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663508-T-C

183378430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663529-C-T

http://identifiers.org/hco/3/GRCh38#183378442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19663541-A-C

183378445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663544-G-A

183378568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19663673-T-C

183378981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19664158-A-G

183379115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19664278-G-T

http://identifiers.org/hco/3/GRCh38#183379227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19664382-C-A

http://identifiers.org/hco/3/GRCh38#183379260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19664415-C-A

183379375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19664524-A-T

http://identifiers.org/hco/3/GRCh38#183379469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19664586-C-A

183379503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664614-T-C

183379559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664645-T-A

183379559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19664645-T-C

183381918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19666108-T-C

183382971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19667954-C-G

183383057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19668041-C-G

183383210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19668179-A-T

183383224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19668193-A-T

183389182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19671777-G-A

http://identifiers.org/hco/3/GRCh38#183389572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19672974-C-A

183389572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19672974-C-T

183389678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19673073-A-T

http://identifiers.org/hco/3/GRCh38#183389694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19673087-A-C

183389808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19673194-G-T

http://identifiers.org/hco/3/GRCh38#183389822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19673208-A-C

183389858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19673245-T-C

183389865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19673252-A-T

http://identifiers.org/hco/3/GRCh38#183389904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19673293-C-A

183389904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19673293-C-T

183390270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19674004-T-C

183390276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19674010-T-A

183390381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/3/GRCh38#183390934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19674768-A-C

183391110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19674912-C-T

http://identifiers.org/hco/3/GRCh38#183392358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19677301-C-A

183392533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19677455-G-T

183392607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19677531-G-A

183392607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19677531-G-C

http://identifiers.org/hco/3/GRCh38#183392631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19677553-C-A

http://identifiers.org/hco/3/GRCh38#183392662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19677584-A-C

183392941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19677852-A-T

183393119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19678032-C-G

183393164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19678063-C-T

183394838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19680189-T-C

183395388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19694792-A-G

183399471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19701792-G-T

183399497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19701818-A-G

183399534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19701853-G-A

183399939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19702088-G-A

183400198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19702316-G-C

183400237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19702341-C-T

183400257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19702364-T-A

183400301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19702410-G-T

183400345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19702437-C-G

183400437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 19702529-G-A

183400470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19702562-C-T

183400509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 19702604-G-A

http://identifiers.org/hco/3/GRCh38#183400751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19702835-C-A

http://identifiers.org/hco/3/GRCh38#183400911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19702958-C-A

183401004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19703052-C-T

183401010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19703059-A-G

183401095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19703123-G-A

183426326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19712659-G-A

183426326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19712659-G-C

183426377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19712710-G-C

http://identifiers.org/hco/3/GRCh38#183427419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19713183-C-A

183427420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713184-G-A

183427424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713188-G-A

183427530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713263-T-C

183427753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713491-G-T

http://identifiers.org/hco/3/GRCh38#183427770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19713513-C-A

http://identifiers.org/hco/3/GRCh38#183427785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19713530-A-C

http://identifiers.org/hco/3/GRCh38#183427792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19713537-A-C

183427792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713537-A-G

183427792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713537-A-T

183427827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron variant
orthologous variants: 19713567-A-G

183427912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 19713642-G-A

183427950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant
orthologous variants: 19713685-G-A

183427950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant
orthologous variants: 19713685-G-C

183427950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant
orthologous variants: 19713685-G-T

183427951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: intron_variant, missense_variant
orthologous variants: 19713686-C-T

183428035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19713756-G-A

183428035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19713756-G-T

183428036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19713757-G-A

183428036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19713757-G-T

http://identifiers.org/hco/3/GRCh38#183428315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19713956-C-A

183428315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19713956-C-T

183428356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19713995-G-A

183428356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19713995-G-C

183428434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714069-C-G

http://identifiers.org/hco/3/GRCh38#183428447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19714078-C-A

183428447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714078-C-T

183428459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714089-G-A

183428459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714089-G-T

183428460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714090-G-A

183428460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714090-G-T

183428466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714096-G-A

183428466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 19714096-G-C

183428606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5 prime UTR variant
orthologous variants: 19714177-G-T

183428621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5 prime UTR variant
orthologous variants: 19714196-A-G

183428621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5 prime UTR variant
orthologous variants: 19714196-A-T

183428674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5 prime UTR variant
orthologous variants: 19714228-T-C

http://identifiers.org/hco/3/GRCh38#183428693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#19714247-C-A

183428693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 19714247-C-T

183428709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5 prime UTR variant
orthologous variants: 19714263-A-G

183428745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 19714292-T-C

183428746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 19714293-G-A

183428746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30319
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 19714293-G-T