http://identifiers.org/hco/19/GRCh38#28883444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39925766-C-A

28883444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925766-C-T

28883588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925907-T-C

28883588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925907-T-G

28883622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925941-G-T

http://identifiers.org/hco/19/GRCh38#28883632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39925951-C-A

28883632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925951-C-T

28883651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925970-C-G

28883651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925970-C-T

28883664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39925983-G-A

28883704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39926019-G-T

28883763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39926087-G-A

28883763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 39926087-G-T

28883861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39926185-G-A

28883882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39926206-A-G

http://identifiers.org/hco/19/GRCh38#28883899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39926223-C-A

28887775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39927769-T-A

28887937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39927927-G-C

28887958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39927948-G-A

28888001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39927991-G-A

28888001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39927991-G-T

28888024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928014-G-C

28888070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928059-T-G

28888080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928069-G-A

28888821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928491-G-A

28888827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928497-C-T

28889198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928756-C-T

28889208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928766-G-A

28889208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928766-G-T

28889314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928872-G-A

28889314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39928872-G-T

http://identifiers.org/hco/19/GRCh38#28889320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39928878-C-A

28889814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39929821-T-C

http://identifiers.org/hco/19/GRCh38#28890289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39930214-C-A

28890289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39930214-C-T

28890457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39930382-T-A

28890652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39930580-C-T

28890757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39930696-A-G

28890870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39930795-C-T

28891512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39931193-C-T

http://identifiers.org/hco/19/GRCh38#28891552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39931234-C-A

28891552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39931234-C-T

28891613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39931292-G-A

28891613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39931292-G-T

28891722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39931383-G-A

http://identifiers.org/hco/19/GRCh38#28893357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39937462-C-A

28893357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39937462-C-T

28893431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39937537-T-C

28893496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39937584-T-C

28893623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39937712-C-T

28894280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39939670-A-G

28895371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39940576-T-A

28895371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39940576-T-C

28895416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39940621-G-T

28895439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39940642-C-T

28899054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39947417-T-C

28899149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39947506-G-A

28899167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39947520-G-A

28899167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39947520-G-T

28899217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39947577-C-T

28900004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39948661-A-G

28900065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39948725-G-C

28900241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39948898-A-G

28900661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39949093-G-A

28900805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39949216-T-C

28902691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951493-C-G

28902701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951503-T-G

28902705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951507-T-C

28902735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951537-G-T

28902752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951554-T-C

28902819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951625-G-A

28902877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951669-G-A

28902961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39951753-T-C

http://identifiers.org/hco/19/GRCh38#28903242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39952119-C-A

28903242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39952119-C-T

28903258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39952137-A-G

28903948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39953192-T-A

28903984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39953220-G-C

28904599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954418-G-A

28904627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954447-G-T

28904894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954737-C-T

28904922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954744-T-C

28904955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954774-G-A

28904955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954774-G-C

28904990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39954801-C-T

28905112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39955267-G-A

28905277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39955430-A-G

28905665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39955792-A-G

28906704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39957861-T-C

28906817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39957971-T-C

28907151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958016-C-G

28907151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958016-C-T

28907157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958022-C-T

28907247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958102-C-T

28907248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958103-C-T

http://identifiers.org/hco/19/GRCh38#28907529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39958374-C-A

28907529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958374-C-T

28907607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958454-C-T

http://identifiers.org/hco/19/GRCh38#28907681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39958521-C-A

28907717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39958562-C-T

28909948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39959815-T-C

28912013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968042-G-T

28912059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968090-G-A

28912059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968090-G-T

28912174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968203-C-T

http://identifiers.org/hco/19/GRCh38#28912339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39968371-C-A

http://identifiers.org/hco/19/GRCh38#28912540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39968556-C-A

28912547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968563-G-C

28912762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968783-A-G

28912790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968811-T-G

28912867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39968886-C-T

28913123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39969115-T-C

28913310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39969310-G-A

28913364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39969343-C-T

28913752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39969879-G-A

28913859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39969986-C-G

http://identifiers.org/hco/19/GRCh38#28914154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39970220-C-A

28914154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39970220-C-G

http://identifiers.org/hco/19/GRCh38#28914471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39970442-C-A

28914606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39970602-G-C

28914645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39970640-A-G

28914702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39970704-T-G

28915313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39970968-A-T

28915370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39971024-G-A

28915468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39971314-A-T

28915481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39971327-G-A

28916513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39972389-G-A

28916528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39972404-G-T

28916592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39972472-A-G

http://identifiers.org/hco/19/GRCh38#28916936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39973986-C-A

28916936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39973986-C-T

28917034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974068-C-G

28917057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974084-G-A

28917057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974084-G-T

28917162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974175-C-G

http://identifiers.org/hco/19/GRCh38#28917279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39974284-C-A

28917320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974338-T-A

28917432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974422-A-G

http://identifiers.org/hco/19/GRCh38#28917535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39974527-C-A

28917963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39974926-C-T

28918102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39975070-A-T

28918288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39975257-C-G

28918288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39975257-C-T

28918317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39975286-G-A

28919151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39976912-T-C

28919692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

http://identifiers.org/hco/19/GRCh38#28920220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39977687-C-A

28920264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39977729-G-A

28920264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39977729-G-T

28920460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39977979-G-C

http://identifiers.org/hco/19/GRCh38#28920647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39978276-C-A

28920647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39978276-C-G

28920711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39978340-T-C

http://identifiers.org/hco/19/GRCh38#28925265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#39981833-C-A

28925498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39982033-C-G

28925731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39982348-T-G

28925735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39982352-G-A

28925918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39982845-T-C

28929262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39996692-T-C

28929262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39996692-T-G

28929449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39996848-A-G

28929496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39996894-G-T

28929780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39996963-C-T

28930081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39997234-T-C

28930565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39997417-G-A

28930662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39997520-T-A

28930956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39997810-T-A

28931232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39997933-A-G

28931260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39997961-G-T

28931449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39998147-G-C

28931605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39998284-T-G

28934619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40000016-T-C

28934691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40000090-A-G

28934826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40000233-G-T

28934864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40000272-G-A

28935570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40000668-G-A

28935579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40000674-C-T

28936179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40001676-C-T

28936287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40001773-A-T

28939465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40004626-G-A

28939465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40004626-G-T

28940323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40004895-G-C

28940420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006063-A-G

28940643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006297-T-A

28940693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006334-G-A

28940743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006383-G-A

28940850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006471-T-C

28941014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006600-A-G

28941014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006600-A-T

28941047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40006629-G-C

28941505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007175-A-G

28941597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007263-C-T

28941704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007378-G-A

28941836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007512-A-G

28942017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007687-G-A

28942371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007998-C-G

http://identifiers.org/hco/19/GRCh38#28942372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40007999-A-C

28942372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40007999-A-G

http://identifiers.org/hco/19/GRCh38#28942438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40008042-C-A

28942469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40008072-A-G

28942582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40008178-G-A

28943444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010598-A-G

28943504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010656-A-G

28943539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010664-C-G

28943587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010698-T-A

28943587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010698-T-G

http://identifiers.org/hco/19/GRCh38#28943612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40010723-C-A

28943664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010775-C-T

28943825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40010913-G-A

28943849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40010935-G-C

28944041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40011185-C-T

28944288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40011474-G-T

28945034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40016554-T-G

28945110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40016562-G-C

28945190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40016637-G-A

28945509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40016961-G-C

28945562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40017002-A-T

28945681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40017115-C-T

28945735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40017161-G-T

28945922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40017352-A-G

28945926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40017356-G-C

28946017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40017488-A-G

28946191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40017657-G-T

28946753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018089-T-C

28946755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018091-A-G

28946818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018190-G-C

28946818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018190-G-T

28946822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018193-A-G

28946910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018278-T-C

28946973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018337-A-G

28947077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018409-A-G

28947173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018512-G-A

28947177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018516-A-G

28947243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018582-C-T

28947489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018798-G-A

http://identifiers.org/hco/19/GRCh38#28947529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40018823-A-C

28947542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40018828-T-C

http://identifiers.org/hco/19/GRCh38#28947663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40018917-A-C

28947799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019039-C-G

28947826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019066-C-T

28947831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019071-G-A

http://identifiers.org/hco/19/GRCh38#28947832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40019072-A-C

28947833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019073-G-A

28947943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019454-C-G

28947943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019454-C-T

28948017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019543-C-G

28948082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019610-G-T

28948222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019750-C-T

28948296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019812-G-A

28948331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40019847-T-C

28948523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020022-C-T

28948607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020446-T-G

28948610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020449-T-C

28948651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020489-G-A

28948651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020489-G-C

28948651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020489-G-T

28948717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020543-A-G

28948717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020543-A-T

28948725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40020551-A-G

28950001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40021873-A-G

28950063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40021920-G-A

28950085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40021946-G-T

28950100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40021961-C-T

28950112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40021973-C-T

http://identifiers.org/hco/19/GRCh38#28950125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40021984-C-A

28950134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40021993-C-T

28950147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40022006-T-C

http://identifiers.org/hco/19/GRCh38#28950214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40022066-C-A

28950214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40022066-C-T

28950324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40022141-G-A

28950324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40022141-G-T

http://identifiers.org/hco/19/GRCh38#28950336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40022153-C-A

28950811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40022559-G-T

28951548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40026718-G-A

28951636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40026811-G-T

28951756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40026926-G-T

28951842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40027000-G-A

28952639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40027734-C-G

28952639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40027734-C-T

28954616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029347-A-T

28954744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029468-T-C

28954747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029471-T-C

28955091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029745-G-A

28955102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029754-A-G

28955105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029757-A-T

28955109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029761-G-A

28955113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029765-C-T

28955248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029852-T-A

28955249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40029853-T-A

28955559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40030133-T-A

28957223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40030909-T-C

28957278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40030963-G-C

28957278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40030963-G-T

28965462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40033486-C-T

28965593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40033622-T-C

28965744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40033776-A-G

28965841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40033863-C-T

http://identifiers.org/hco/19/GRCh38#28965847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40033869-A-C

28966099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034093-A-G

28966161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034318-A-G

http://identifiers.org/hco/19/GRCh38#28966319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034449-C-A

http://identifiers.org/hco/19/GRCh38#28966330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034461-C-A

28966356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034474-C-T

28966358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034476-A-G

28966453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034570-C-T

http://identifiers.org/hco/19/GRCh38#28966456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034573-A-C

28966456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034573-A-G

28966470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40034579-A-G

28966602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034684-G-A

http://identifiers.org/hco/19/GRCh38#28966700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034759-C-A

28966709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034765-C-T

http://identifiers.org/hco/19/GRCh38#28966716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034772-C-A

http://identifiers.org/hco/19/GRCh38#28966759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034801-C-A

28966762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034804-A-G

28966781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034822-A-T

28966799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034840-T-C

28966803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034844-G-T

28966852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034902-T-C

28966873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034929-G-A

http://identifiers.org/hco/19/GRCh38#28966894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40034956-C-A

28966894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40034956-C-T

28967183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036214-T-C

http://identifiers.org/hco/19/GRCh38#28967191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40036222-C-A

28967196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036227-C-T

28967197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036228-G-A

28967229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40036256-A-G

28967237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036264-G-A

28967237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036264-G-T

28967255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036282-T-A

28967255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036282-T-C

http://identifiers.org/hco/19/GRCh38#28967346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40036351-C-A

28967346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036351-C-T

28967395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036401-C-T

28967486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036492-T-A

28967486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036492-T-C

28967501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036507-G-A

28967501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40036507-G-T

28968113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40037806-G-A

28968113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40037806-G-T

28968184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40037874-G-A

28968207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40037893-A-T

28968375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038008-G-T

28968377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038010-G-T

28968418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038039-A-G

28968481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038079-G-A

28968481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038079-G-T

http://identifiers.org/hco/19/GRCh38#28968626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40038129-A-C

28968626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038129-A-G

28968806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038299-A-G

28968988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038436-G-A

http://identifiers.org/hco/19/GRCh38#28968990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40038438-C-A

http://identifiers.org/hco/19/GRCh38#28968991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40038439-C-A

28968991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40038439-C-T

http://identifiers.org/hco/19/GRCh38#28969162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40038596-C-A

28969173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40038608-G-A

28969173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40038608-G-C

28969173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40038608-G-T

http://identifiers.org/hco/19/GRCh38#28969282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40038694-C-A

28969535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40038837-G-T

28969541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40038843-A-T

28969578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40038945-G-A

28969636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40039004-A-G

http://identifiers.org/hco/19/GRCh38#28969648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#40039010-C-A

28969648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40039010-C-G

28969697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27121
most severe consequence: non coding transcript exon variant
orthologous variants: 40039062-G-T