http://identifiers.org/hco/20/GRCh38#62816464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180239562-C-A

62816924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180239904-C-T

62816968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180239949-G-A

62816968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180239949-G-T

62816992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180239973-G-A

62816992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180239973-G-T

http://identifiers.org/hco/20/GRCh38#62817001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180239985-A-C

http://identifiers.org/hco/20/GRCh38#62817020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240004-C-A

62817020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180240004-C-T

http://identifiers.org/hco/20/GRCh38#62817031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240015-C-A

62817031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180240015-C-G

62817031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180240015-C-T

http://identifiers.org/hco/20/GRCh38#62817042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240029-C-A

62817042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180240029-C-T

http://identifiers.org/hco/20/GRCh38#62817122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240098-C-A

62817122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 180240098-C-G

62817122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180240098-C-T

http://identifiers.org/hco/20/GRCh38#62817182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240174-C-A

62817182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 180240174-C-T

62817402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 180240481-G-A

http://identifiers.org/hco/20/GRCh38#62817439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240519-C-A

62817439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 180240519-C-G

62817439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 180240519-C-T

http://identifiers.org/hco/20/GRCh38#62817468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180240562-C-A

62817468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180240562-C-G

62817468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180240562-C-T

62817528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180240621-G-A

62817528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180240621-G-T

62817530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180240623-G-A

62817530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180240623-G-C

62817530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180240623-G-T

62817998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180240979-T-C

62818017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180240998-G-C

62818069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241057-G-A

62818073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241061-T-G

62818129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241146-C-T

62818147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241164-T-C

62818367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241443-A-G

62818370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241446-T-C

62818370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241446-T-G

62818378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241454-G-A

62818378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241454-G-T

62818382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241467-G-A

http://identifiers.org/hco/20/GRCh38#62818383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180241468-C-A

62818383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241468-C-T

http://identifiers.org/hco/20/GRCh38#62818386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180241471-A-C

62818386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241471-A-G

62818386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241471-A-T

62818658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241931-G-A

62818658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241931-G-T

62818667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180241940-G-T

62818806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242017-G-A

62818806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242017-G-C

62818806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242017-G-T

62819050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242195-C-T

http://identifiers.org/hco/20/GRCh38#62819186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180242279-C-A

62819186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242279-C-G

62819186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242279-C-T

http://identifiers.org/hco/20/GRCh38#62819204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180242297-C-A

62819204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242297-C-T

62819310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242408-C-G

62819345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242439-T-A

62819346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242440-G-T

http://identifiers.org/hco/20/GRCh38#62819421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180242516-C-A

http://identifiers.org/hco/20/GRCh38#62819422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180242517-A-C

62819422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242517-A-G

62819663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180242952-C-T

http://identifiers.org/hco/20/GRCh38#62819841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180243284-A-C

62820090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180243523-A-G

62820115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180243561-G-T

62820148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180243583-T-C

62820384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180243772-G-A

62820384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180243772-G-C

62820597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180243912-G-T

62820843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244116-G-A

62821093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244344-G-T

62821111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244361-T-G

62821150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244394-C-G

62821150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244394-C-T

62821162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244417-G-A

62821162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244417-G-T

http://identifiers.org/hco/20/GRCh38#62821240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180244487-C-A

62821240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244487-C-G

62821240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244487-C-T

62821322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244671-T-C

http://identifiers.org/hco/20/GRCh38#62821388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180244777-C-A

62821388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244777-C-G

62821388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244777-C-T

62821457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244860-G-A

62821457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244860-G-T

62821577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244964-G-A

62821595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180244998-G-A

62821608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245011-G-A

62821730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245124-T-A

62821828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245221-A-G

http://identifiers.org/hco/20/GRCh38#62821833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180245226-C-A

62821879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245272-A-G

62821879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245272-A-T

http://identifiers.org/hco/20/GRCh38#62821907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180245315-C-A

62821907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245315-C-T

62822014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245453-G-A

62822014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245453-G-T

http://identifiers.org/hco/20/GRCh38#62822032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180245470-C-A

62822032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245470-C-T

62822086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245517-T-C

http://identifiers.org/hco/20/GRCh38#62822102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180245533-C-A

62822102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245533-C-G

62822102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245533-C-T

62822295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245707-G-A

62822295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245707-G-T

62822325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245729-G-C

62822455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180245830-G-A

62822523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 180245889-G-A

62822523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 180245889-G-T

62824315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180246907-T-A

62824315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180246907-T-C

62824315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180246907-T-G

62824332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180246924-G-C

62824332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180246924-G-T

http://identifiers.org/hco/20/GRCh38#62824343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180246935-C-A

62824343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180246935-C-T

62824462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180247028-G-A

62824462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180247028-G-T

62824492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180247058-A-G

62824492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180247058-A-T

http://identifiers.org/hco/20/GRCh38#62824529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180247099-C-A

62824529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247099-C-T

62824547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247113-A-G

http://identifiers.org/hco/20/GRCh38#62824578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180247143-A-C

62824608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247173-T-A

62824608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247173-T-C

62824608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247173-T-G

62824625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247190-G-A

62824625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247190-G-T

62824650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247199-T-G

62824655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247204-C-T

62824680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247236-A-T

62824690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247246-G-A

62824757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247312-G-A

http://identifiers.org/hco/20/GRCh38#62824854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180247395-C-A

62824854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247395-C-T

http://identifiers.org/hco/20/GRCh38#62824859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180247400-C-A

62824859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247400-C-T

62824884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247423-G-A

http://identifiers.org/hco/20/GRCh38#62824888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180247427-C-A

62825313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247762-C-G

62825372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247807-G-A

62825372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180247807-G-T

62825515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180247965-G-A

62825549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248000-G-T

http://identifiers.org/hco/20/GRCh38#62825555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180248006-C-A

62825555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248006-C-T

62825576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248027-G-A

62825576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248027-G-T

62825577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248028-G-T

62825613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248063-C-G

62825613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248063-C-T

http://identifiers.org/hco/20/GRCh38#62825645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180248095-C-A

62825645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180248095-C-T

http://identifiers.org/hco/20/GRCh38#62825700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180248152-A-C

62825700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248152-A-G

62825760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248214-G-A

62825760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248214-G-C

62825774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248226-G-A

62825834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180248285-T-C

62825834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180248285-T-G

62825893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248344-A-G

62825893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248344-A-T

62825952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248381-G-A

62825952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248381-G-T

62826044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248446-C-G

http://identifiers.org/hco/20/GRCh38#62826061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180248463-C-A

62826061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248463-C-T

62826121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248521-G-A

62826121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248521-G-T

http://identifiers.org/hco/20/GRCh38#62826219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180248616-C-A

62826219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 180248616-C-G

62826219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 180248616-C-T

62826242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180248639-G-A

62826242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180248639-G-C

62826242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180248639-G-T

http://identifiers.org/hco/20/GRCh38#62826336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180248703-C-A

62826336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248703-C-G

62826336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248703-C-T

62826372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248739-G-A

62826372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248739-G-T

62826423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248763-G-A

62826423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248763-G-T

62826456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248774-T-C

62826682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248811-G-A

62826691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248820-G-A

62826691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248820-G-T

62826839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248953-G-A

62826839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248953-G-C

62826839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180248953-G-T

62826960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249096-T-A

62827094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249314-A-G

62827226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249405-C-G

62827226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249405-C-T

62827229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249408-C-T

62827236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 180249415-T-C

62827371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249545-G-A

62827371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249545-G-T

http://identifiers.org/hco/20/GRCh38#62827403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180249593-C-A

62827403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249593-C-G

62827403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249593-C-T

http://identifiers.org/hco/20/GRCh38#62827495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180249690-A-C

62827495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249690-A-G

62827591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180249889-G-A

62827775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180250046-G-A

62827775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180250046-G-T

http://identifiers.org/hco/20/GRCh38#62827812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180250087-C-A

62827812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180250087-C-T

http://identifiers.org/hco/20/GRCh38#62827813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180250088-C-A

62827813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180250088-C-T

62827901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180250205-C-T

62828276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180250604-G-A

62828827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180251182-G-C

http://identifiers.org/hco/20/GRCh38#62828945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180251296-C-A

62828945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 180251296-C-T

62829245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180251525-A-G

62829349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180251643-G-A

62829349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180251643-G-T

62829384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180251673-G-A

62829384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180251673-G-T

62829438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180251832-A-G

http://identifiers.org/hco/20/GRCh38#62829696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180252051-C-A

62829696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252051-C-T

62829713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252166-C-T

http://identifiers.org/hco/20/GRCh38#62829754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180252441-C-A

62829754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252441-C-G

62829754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252441-C-T

62829826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 180252513-G-A

62829826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 180252513-G-T

62829956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252602-T-C

http://identifiers.org/hco/20/GRCh38#62830059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180252709-C-A

62830134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252799-C-T

62830196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252867-C-T

http://identifiers.org/hco/20/GRCh38#62830268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180252951-C-A

62830268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180252951-C-T

http://identifiers.org/hco/20/GRCh38#62830386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180253079-C-A

62830386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: synonymous variant
orthologous variants: 180253079-C-G

62830386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: synonymous variant
orthologous variants: 180253079-C-T

62830416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253109-G-A

62830416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253109-G-T

62830471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253168-A-G

62830481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253178-G-A

http://identifiers.org/hco/20/GRCh38#62830488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180253189-C-A

62830488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253189-C-T

62830505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253206-C-T

http://identifiers.org/hco/20/GRCh38#62830836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180253390-C-A

62831060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253534-G-A

62831060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron variant
orthologous variants: 180253534-G-T

62831204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 180253638-T-C

62831204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 180253638-T-G

62831232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 180253667-G-A

62831658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 180254071-G-C

62831658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 180254071-G-T

62832108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180254703-G-C

http://identifiers.org/hco/20/GRCh38#62832146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180254741-A-C

62832146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 180254741-A-T

62832192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254785-G-A

62832207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254798-T-C

62832208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254799-G-T

62832213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254804-A-G

http://identifiers.org/hco/20/GRCh38#62832246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180254813-C-A

62832246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254813-C-T

62832282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254836-G-T

http://identifiers.org/hco/20/GRCh38#62832299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180254856-C-A

62832303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254860-C-G

62832303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254860-C-T

62832304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254861-T-C

62832351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254895-C-G

62832368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180254917-G-A

http://identifiers.org/hco/20/GRCh38#62832374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180254923-A-C

62832889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180255843-G-A

62832889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180255843-G-T

http://identifiers.org/hco/20/GRCh38#62833093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180256011-C-A

62834449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180256342-C-T

62834559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180256453-C-G

http://identifiers.org/hco/20/GRCh38#62834610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180256504-A-C

62835626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180256837-G-A

62835761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180256925-T-C

62835796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180256961-G-C

62835964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180257124-G-A

62835964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180257124-G-C

62835976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180257136-G-A

62836048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 180257187-G-A

http://identifiers.org/hco/20/GRCh38#62836415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180257536-C-A

62836415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180257536-C-T

62836522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180257640-G-A

62836522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180257640-G-C

62836522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 180257640-G-T

http://identifiers.org/hco/20/GRCh38#62837064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180258155-C-A

62837064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 180258155-C-T

62837228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180258319-C-T

http://identifiers.org/hco/20/GRCh38#62837356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180258676-C-A

62837356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258676-C-G

62837356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258676-C-T

62837365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258686-G-T

62837366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258687-G-A

62837370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258691-A-G

62837377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258698-G-A

62837377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258698-G-T

62837385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258706-G-A

62837679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258968-C-G

62837679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258968-C-T

62837691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180258980-C-T

62837748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180259021-A-G

http://identifiers.org/hco/20/GRCh38#62838674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180261476-C-A

62838674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180261476-C-T

62838872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 180261618-G-C

62840714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 180263195-A-G

http://identifiers.org/hco/20/GRCh38#62840748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180263236-A-C

http://identifiers.org/hco/20/GRCh38#62840757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180263260-C-A

62840757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180263260-C-T

62840796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180263292-G-A

62840796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180263292-G-T

62840872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180263366-G-A

62840872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180263366-G-T

http://identifiers.org/hco/20/GRCh38#62840939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#180263447-A-C

62840939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2219
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 180263447-A-G