http://identifiers.org/hco/2/GRCh38#42169369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658396-C-A

42169369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83658396-C-G

42169369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83658396-C-T

http://identifiers.org/hco/2/GRCh38#42169391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658436-A-C

42169391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83658436-A-G

42169462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 83658494-G-T

42169520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83658552-G-A

42169520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83658552-G-C

42169520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83658552-G-T

42169527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83658559-T-C

42169668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83658700-G-A

42169668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83658700-G-C

42169668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83658700-G-T

http://identifiers.org/hco/2/GRCh38#42169694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658730-C-A

42169694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83658730-C-T

http://identifiers.org/hco/2/GRCh38#42169700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658736-C-A

42169700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83658736-C-G

42169700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83658736-C-T

http://identifiers.org/hco/2/GRCh38#42169791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658826-C-A

42169791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83658826-C-G

42169791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83658826-C-T

http://identifiers.org/hco/2/GRCh38#42169918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658928-C-A

42169918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83658928-C-T

http://identifiers.org/hco/2/GRCh38#42169969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83658977-C-A

42169969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 83658977-C-G

42169969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 83658977-C-T

42170038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83659044-T-A

42170038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83659044-T-C

42170038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83659044-T-G

42170206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83659184-A-G

42170358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659306-T-A

42170358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659306-T-C

42170382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659330-T-C

42170382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659330-T-G

42170390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659338-C-T

42170651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659595-A-G

42170675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659615-A-G

42170857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659811-A-G

42170861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659815-A-G

42170955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83659910-A-G

42171206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83660174-A-G

42171970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83660752-G-C

42172103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83660874-G-A

42172131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83660901-C-G

42172689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83661398-A-G

42172718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83661427-T-A

42172807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83661524-C-T

42172854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83661568-A-T

42172877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83661593-A-G

42173400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83662877-G-A

42173400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83662877-G-C

42173459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83662931-T-C

42173941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83663098-A-G

42173980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83663140-G-T

http://identifiers.org/hco/2/GRCh38#42174073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83663249-C-A

42174297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83663465-G-C

42174297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83663465-G-T

42177698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83664956-G-C

http://identifiers.org/hco/2/GRCh38#42177865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83665106-C-A

42177865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83665106-C-T

42177884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83665122-A-G

42178003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83665241-G-C

42178127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83665298-A-G

42179152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666148-A-G

42179154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666150-A-G

42179394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666247-C-T

42179634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666453-G-A

42179634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666453-G-C

42179727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666520-C-G

42179727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666520-C-T

42179745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83666534-G-C

42180153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83667007-A-T

42180215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83667068-C-T

42180270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83667123-C-T

42180287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83667140-T-C

42180312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83667165-G-A

42183156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674307-A-G

42183187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674337-T-A

42183277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674444-C-T

http://identifiers.org/hco/2/GRCh38#42183278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83674445-A-C

42183278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674445-A-G

42183278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674445-A-T

42183370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83674528-A-G

http://identifiers.org/hco/2/GRCh38#42183382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83674540-A-C

42183382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674540-A-G

42183388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674546-G-A

http://identifiers.org/hco/2/GRCh38#42183651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83674790-C-A

42183651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674790-C-T

42183798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83674870-C-T

42184021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83675088-A-G

42184577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83675594-C-G

42185252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83676848-T-C

42193529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83681929-A-G

42193529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83681929-A-T

42193732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83681998-C-T

42194854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83683206-G-C

42194872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83683232-A-G

42195163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83683559-T-A

42195290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83683652-T-G

42196065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83684699-T-G

42196619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83685441-A-G

42196626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83685448-T-C

42199281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83685698-C-T

42199746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686087-G-C

42199770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686111-G-A

42199789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686125-G-A

42199969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686274-T-A

42200547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686486-A-G

42200595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686520-G-T

42200741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686660-G-A

42200790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686704-A-G

42201019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83686904-A-T

42204566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83688208-T-G

42204852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83688417-G-A

42204960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83688520-A-G

42205256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83689232-C-G

42205371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83689348-G-C

42205755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83689688-A-G

42206591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691227-T-C

42206852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691403-A-G

42206903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83691450-T-C

42216996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693490-G-A

42216996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83693490-G-C

42217584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694584-A-G

42217646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694630-C-T

42217663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83694646-G-A

http://identifiers.org/hco/2/GRCh38#42226815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83697554-A-C

42226836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83697573-T-C

42229213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83698460-T-G

42230042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83700325-C-G

42230042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83700325-C-T

42230070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83700359-G-C

42230156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83700530-T-G

42230684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701724-G-A

42230716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83700765-C-G

42230933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701574-T-G

42230985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701526-A-G

http://identifiers.org/hco/2/GRCh38#42230996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83701515-A-C

42230996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701515-A-G

42231015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701495-C-G

42231048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701475-C-T

42231056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701467-C-G

http://identifiers.org/hco/2/GRCh38#42231500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83701160-A-C

42231500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701160-A-T

42231510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701150-T-C

42231616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83701042-C-T

42233317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83704372-T-C

42233407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83704454-A-G

42233627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83704659-G-A

42233636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83704668-G-A

42233808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83704799-G-A

42234068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83705026-A-G

42234664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83705556-A-G

42234852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83705783-C-G

http://identifiers.org/hco/2/GRCh38#42235586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83708542-A-C

42235689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83708636-C-T

http://identifiers.org/hco/2/GRCh38#42235784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83708712-A-C

42235785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83708713-T-C

42239248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83712479-A-G

42239309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83712539-T-G

42239516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83712701-T-C

42239993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83713011-A-G

42240000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83713015-C-T

42240003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83713018-G-A

42240118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83713130-A-G

42240125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83713137-G-A

42242467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83714888-T-G

http://identifiers.org/hco/2/GRCh38#42243477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83715999-A-C

42243519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83716037-C-T

42243858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83716356-A-G

42244098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83716704-T-G

42245581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83717531-A-G

42245794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83717723-A-G

42250023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83720982-C-T

42251396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83721388-T-A

42251530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83721501-A-G

42251531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83721502-G-A

42251599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83721567-C-G

42255604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83721856-T-G

http://identifiers.org/hco/2/GRCh38#42255738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83721982-A-C

42255989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83722313-A-G

42256223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83722461-G-A

42256245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83722478-T-C

42256357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83722593-G-A

http://identifiers.org/hco/2/GRCh38#42256380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83722612-C-A

42256380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83722612-C-G

42256472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729008-A-T

http://identifiers.org/hco/2/GRCh38#42256694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83729228-C-A

42256694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729228-C-G

42256694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729228-C-T

42256719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729251-G-A

42256738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729271-G-A

42256738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729271-G-C

42256738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729271-G-T

42257294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729740-C-T

42257344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729810-C-T

42257466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83729886-G-A

42258117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730420-C-T

42258411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730682-A-G

42258411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730682-A-T

42258440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730711-G-A

42258481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730755-A-G

42258481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730755-A-T

42258534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83730791-G-A

42260686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83732181-G-A

42260802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83732412-T-G

42260991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83732573-T-C

42260996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83732578-A-G

42261418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 83732962-T-G

42261808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83733324-A-T

http://identifiers.org/hco/2/GRCh38#42261950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83733465-C-A

42262132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83733649-T-C

42262861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83734338-T-G

42262892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83734371-G-A

http://identifiers.org/hco/2/GRCh38#42262944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83734422-C-A

42264570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83735305-A-G

http://identifiers.org/hco/2/GRCh38#42264624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83735359-C-A

42264624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83735359-C-G

42264624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83735359-C-T

42264725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense variant
orthologous variants: 83735448-A-G

42264762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83735482-T-C

42264881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83735608-T-C

42264946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, missense_variant
orthologous variants: 83735672-G-A

42265559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83735828-C-T

42265830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83736086-C-G

42266183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83736425-T-C

42266318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83736547-T-C

42266427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83736681-C-T

42266460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83736725-G-C

42267575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83737701-G-A

42267575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83737701-G-T

42267752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83737859-A-G

42267877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83737958-A-G

42267964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83738039-C-T

42269256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739230-T-C

42269257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739231-T-G

42269258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739232-T-C

42269312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739288-A-G

42269481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739457-G-A

42269481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739457-G-C

42269541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739529-G-C

42269977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739850-G-T

42272337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83739952-T-C

42272388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83740008-C-T

42273484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83740618-C-G

42273484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83740618-C-T

42274022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83741397-G-C

42274080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83741447-C-G

42275587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83742765-T-C

42276026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83743325-G-C

42276235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83743671-G-A

42276273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83743708-T-C

42276791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83744264-A-G

42277115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83744507-A-G

42277120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83744512-G-A

42277174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83744568-C-T

http://identifiers.org/hco/2/GRCh38#42277300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83744688-A-C

42277337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83744717-G-A

42277337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83744717-G-C

42277722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745054-C-T

42277810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745135-G-C

42277950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745243-A-G

42278108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745352-G-C

42278108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745352-G-T

42278184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745416-A-G

42278994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745737-T-G

42279105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83745856-T-C

42279168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746252-A-G

42279373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746445-G-C

42279377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746449-T-G

42279390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746457-T-C

42279416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746464-G-A

42279459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746494-G-A

42280017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746955-A-G

42280030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746968-G-T

42280046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83746983-G-A

42280142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747083-A-G

42280155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747096-A-T

42280180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747117-C-G

42280299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747218-A-G

http://identifiers.org/hco/2/GRCh38#42280807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83747417-C-A

42280807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747417-C-T

42280948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense variant
orthologous variants: 83747558-C-T

42280950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: synonymous variant
orthologous variants: 83747560-T-C

42281076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747685-G-A

42281076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747685-G-T

42281432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747752-C-T

42281560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747876-G-A

42281560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747876-G-T

42281632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83747933-A-G

42281814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83748245-C-G

http://identifiers.org/hco/2/GRCh38#42281816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83748247-A-C

42281939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83748290-C-G

42281995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83748342-A-G

42282318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron variant
orthologous variants: 83748579-A-G

42282880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense variant
orthologous variants: 83748782-A-T

http://identifiers.org/hco/2/GRCh38#42282892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83748794-C-A

42282892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: synonymous variant
orthologous variants: 83748794-C-T

42283205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83749311-C-T

42283248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83749351-G-A

42283283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83749386-T-G

42284175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751639-G-T

http://identifiers.org/hco/2/GRCh38#42284224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83751684-A-C

42284224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751684-A-T

42284239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751700-G-A

42284249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751707-G-A

42284275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751733-T-G

42284318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751774-C-T

42284379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751812-C-T

http://identifiers.org/hco/2/GRCh38#42284563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83751983-A-C

42284563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83751983-A-G

42286116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83753040-A-G

42286949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83754364-A-G

42287142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83754696-A-G

42287174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83754726-C-T

42287321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83754863-G-T

42288094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83755535-G-A

42288108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83755539-T-G

42288350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83755712-G-T

42288383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83755737-T-C

42288383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83755737-T-G

http://identifiers.org/hco/2/GRCh38#42288388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83755742-C-A

42288388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83755742-C-G

42288388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83755742-C-T

http://identifiers.org/hco/2/GRCh38#42288539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83755869-A-C

42288539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83755869-A-T

http://identifiers.org/hco/2/GRCh38#42288791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83756089-C-A

42288861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83756150-A-G

42288861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83756150-A-T

42288889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83756179-G-A

42288889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83756179-G-T

http://identifiers.org/hco/2/GRCh38#42289321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83756748-A-C

42289321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83756748-A-G

42290250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83757150-C-G

http://identifiers.org/hco/2/GRCh38#42290358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83757251-C-A

42290358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83757251-C-T

42292091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83754696-A-G

42294844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83757786-C-T

42295029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83757984-T-C

42295029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83757984-T-G

42295035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83757990-T-C

42295341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83758331-G-A

42295369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83758356-G-A

42295377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83758364-G-A

42295377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83758364-G-T

42295464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83758451-G-A

42295464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83758451-G-T

42295509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83758496-A-T

42295841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83758703-A-G

42298302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83759101-G-A

42298477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83759266-A-G

42298900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83759917-A-G

42298941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83759959-T-G

42299309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760258-G-A

42299678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760494-T-C

42299702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760512-T-G

42299730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760536-C-T

42299887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760622-T-C

42300121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760748-A-G

42300196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760832-G-A

42300245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760880-A-G

42300246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760881-T-C

42300253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760888-G-A

42300291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83760929-A-G

http://identifiers.org/hco/2/GRCh38#42300305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83760947-A-C

42301029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83761612-A-G

42301130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83761713-T-C

42301399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83761988-A-G

42301399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83761988-A-T

42302912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763260-G-C

42303002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763355-G-A

42303002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763355-G-C

42303002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763355-G-T

42303033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763386-T-C

42303042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763396-G-A

42303050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763406-T-C

42303142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83763499-A-G

42303172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83763529-A-G

42303172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83763529-A-T

42303488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763829-C-G

42303488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763829-C-T

42303550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763865-T-A

42303550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763865-T-C

42303553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83763868-A-T

42304020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764007-A-G

42304043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764026-A-G

42304146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764117-C-T

42304238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764186-C-G

http://identifiers.org/hco/2/GRCh38#42304333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83764257-C-A

42304333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764257-C-T

http://identifiers.org/hco/2/GRCh38#42304357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83764281-C-A

42304357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764281-C-T

http://identifiers.org/hco/2/GRCh38#42304424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83764361-A-C

42304424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764361-A-G

42304425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83764362-C-G

42304540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83764480-G-A

42304540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83764480-G-T

42307471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83765108-A-G

http://identifiers.org/hco/2/GRCh38#42310696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83766160-A-C

42311670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768319-T-A

42311703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768350-G-C

42311703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768350-G-T

42315893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768880-A-G

42315917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768904-A-T

42315936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768923-A-G

42315944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83768935-A-G

42316049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 83769045-A-G

42316077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769071-A-G

http://identifiers.org/hco/2/GRCh38#42316105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83769089-A-C

42316105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769089-A-G

42316105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769089-A-T

42316110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769094-A-G

42316126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769106-T-C

http://identifiers.org/hco/2/GRCh38#42316127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83769107-A-C

42316127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769107-A-G

42316308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769269-C-G

42316332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769282-A-G

http://identifiers.org/hco/2/GRCh38#42316373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83769319-A-C

42316440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769448-C-G

http://identifiers.org/hco/2/GRCh38#42316465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83769471-C-A

42316494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83769503-A-G

42317183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770691-C-T

42317263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770759-G-C

http://identifiers.org/hco/2/GRCh38#42317282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83770777-A-C

42317282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770777-A-G

42317286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770781-T-A

http://identifiers.org/hco/2/GRCh38#42317287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83770782-A-C

42317323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770817-A-G

42317323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770817-A-T

42317324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83770818-G-T

42317560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771069-G-A

42317560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771069-G-T

http://identifiers.org/hco/2/GRCh38#42317575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83771080-C-A

42317575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771080-C-G

42317575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771080-C-T

42317599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771110-A-G

42317600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771111-T-C

42318073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83771819-G-A

http://identifiers.org/hco/2/GRCh38#42318099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83771847-A-C

42318642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83773478-T-G

42319055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83774030-G-A

42319097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83774097-A-G

42319486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83774525-C-T

42319546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83774563-T-C

42319598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 83774599-T-C

42321105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83775717-C-T

http://identifiers.org/hco/2/GRCh38#42321172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83775797-A-C

42321843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83777973-A-G

42321891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778013-G-C

42322016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778127-A-G

42322120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778221-A-G

42322718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83778723-C-G

42323145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83779259-C-G

42323351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83779409-A-G

http://identifiers.org/hco/2/GRCh38#42323397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83779449-A-C

http://identifiers.org/hco/2/GRCh38#42324724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83779777-C-A

42324807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83779853-C-T

42325094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780020-A-G

42325119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780045-T-C

42325119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780045-T-G

42325226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780142-A-G

http://identifiers.org/hco/2/GRCh38#42325270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83780186-A-C

42325285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780206-T-C

42325322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780269-G-A

42325322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780269-G-C

42325322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780269-G-T

42325342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780283-A-G

42325357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780298-C-T

42325378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780316-T-G

42325379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780317-G-A

42325379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780317-G-T

42325385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780323-A-G

42325392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780351-G-C

42325392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780351-G-T

http://identifiers.org/hco/2/GRCh38#42325481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#83780489-C-A

42325481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83780489-C-T

http://identifiers.org/hco/2/GRCh38#42325508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83780516-C-A

42325508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83780516-C-G

42325778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780711-C-G

42325845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780777-T-A

42325920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780849-T-G

42325984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780913-A-T

42326009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780932-T-A

42326009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780932-T-C

42326023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83780946-A-T

http://identifiers.org/hco/2/GRCh38#42326042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83780966-C-A

42326042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 83780966-C-T

42326051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83780975-G-C

42326051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 83780975-G-T

42326056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 83780980-T-C

42326088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83781012-A-G

42326088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83781012-A-T

http://identifiers.org/hco/2/GRCh38#42326101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83781025-A-C

42326101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 83781025-A-G

42326322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83781246-A-G

42326501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83781815-G-A

42328869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83784621-G-A

42328869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83784621-G-T

42328887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 83784634-T-C

http://identifiers.org/hco/2/GRCh38#42328890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83784637-C-A

42328890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83784637-C-G

42328890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83784637-C-T

42328902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83784649-A-T

42328965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83784712-C-G

42328965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83784712-C-T

42329069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83784780-A-G

http://identifiers.org/hco/2/GRCh38#42329131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83784806-A-C

42329586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83784995-A-G

42329586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83784995-A-T

42329606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785015-T-A

42329686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785094-G-A

42329686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 83785094-G-T

42329829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785230-C-G

42329829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83785230-C-T

42329850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83785251-A-G

42329885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785286-C-G

42329886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83785287-T-C

42329887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785288-G-A

42329887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785288-G-C

http://identifiers.org/hco/2/GRCh38#42329913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83785314-C-A

42329913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83785314-C-G

42329913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83785314-C-T

42329943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 83785344-A-G

42329943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785344-A-T

42329944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785345-T-C

42329944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785345-T-G

42329950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785351-A-T

42330074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785463-G-A

42330074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785463-G-C

42330100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 83785489-G-A

42330243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785623-G-A

42330255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785635-G-C

42330255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785635-G-T

42330303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785685-G-C

42330303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785685-G-T

42330331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785712-G-A

42330331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785712-G-C

42330331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785712-G-T

42330337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785718-T-G

http://identifiers.org/hco/2/GRCh38#42330340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83785721-A-C

42330348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785729-T-A

http://identifiers.org/hco/2/GRCh38#42330404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83785784-A-C

42330404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785784-A-G

42330553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785914-T-A

42330597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785968-T-A

42330597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83785968-T-C

http://identifiers.org/hco/2/GRCh38#42330679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83786043-C-A

42330679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786043-C-G

42330695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786058-T-G

http://identifiers.org/hco/2/GRCh38#42330712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83786072-A-C

42330756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786117-T-C

42330787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786148-A-T

42330853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786216-A-G

42331021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786373-G-T

42331067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786423-T-C

42331067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786423-T-G

42331099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786450-T-C

42331248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786563-G-C

42331248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786563-G-T

42331257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786568-G-A

42331397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83786705-A-G

http://identifiers.org/hco/2/GRCh38#42331864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83787108-C-A

42331864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83787108-C-G

42331864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83787108-C-T

http://identifiers.org/hco/2/GRCh38#42331905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#83787150-C-A

42332181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 1316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 83787415-A-G