152780043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84489894-G-A

http://identifiers.org/hco/4/GRCh38#152780123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#84489825-C-A

152780146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84489802-T-C

152780183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 84489765-A-G

http://identifiers.org/hco/4/GRCh38#152780315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84489638-C-A

152780315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84489638-C-T

http://identifiers.org/hco/4/GRCh38#152780345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84489608-C-A

152780345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84489608-C-G

152780923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84489061-C-T

152780994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488990-C-G

152781069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488915-A-G

152781181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488808-T-C

152781254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488746-G-A

152781254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488746-G-C

152781254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488746-G-T

http://identifiers.org/hco/4/GRCh38#152781259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84488741-A-C

152781259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488741-A-G

152781259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488741-A-T

152781265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488735-T-C

http://identifiers.org/hco/4/GRCh38#152781266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84488734-C-A

152781266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488734-C-T

152782299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488262-A-G

152782339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84488223-C-T

152782763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84487835-C-T

152783722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84487015-A-G

152783784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84486954-T-A

152786229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84486016-T-G

152786613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84485654-C-G

152786622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84485645-A-G

152786968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484636-A-G

152786999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484612-T-C

152787012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484599-G-A

152787089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484565-A-G

152787113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484538-A-G

http://identifiers.org/hco/4/GRCh38#152787130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84484521-A-C

152787130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484521-A-G

152787219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84484427-C-T

152789747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84483260-C-T

152789776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84483244-T-A

http://identifiers.org/hco/4/GRCh38#152789782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84483238-C-A

152789836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84483189-T-A

152789925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84483092-C-T

http://identifiers.org/hco/4/GRCh38#152790248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84482791-C-A

152790616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84482413-T-C

152790713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84482327-G-A

152790713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84482327-G-T

152791277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84482122-G-A

152791281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84482118-A-G

152791466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84481943-T-C

152792171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84481752-C-G

152792364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84480111-T-G

152792487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84479991-C-T

152793051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84479147-A-G

152798947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84473675-C-T

152800314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471932-G-A

http://identifiers.org/hco/4/GRCh38#152800539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84471756-C-A

152800814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471505-G-T

152800871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471450-G-T

152800949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471381-A-G

152800984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471336-G-C

152801000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471321-G-T

152801246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471105-G-A

152801321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471036-G-C

152801331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84471026-G-A

152801399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84470968-C-T

152801469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84470824-G-A

152801582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84470694-C-T

152801617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84470659-G-C

152802040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469063-A-G

152802275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469299-T-A

152802276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469300-G-A

152802394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469413-A-G

152802646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469668-G-A

152802660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469693-C-G

152802745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84469781-T-C

152803069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466916-G-A

152803317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466682-T-C

152803350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466653-A-G

http://identifiers.org/hco/4/GRCh38#152804613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84466506-C-A

152804725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466444-A-G

152804959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466259-T-A

152804959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466259-T-C

152805053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84466163-A-G

152805966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84465893-A-G

152806016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84465836-C-T

152806032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84465820-C-T

152806141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84465716-G-A

152806398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84465474-C-G

152809480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461596-T-G

152809526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461559-G-T

http://identifiers.org/hco/4/GRCh38#152809589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84461523-C-A

152809590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461522-C-T

http://identifiers.org/hco/4/GRCh38#152809637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84461487-C-A

152809923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461054-A-G

152809932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461045-G-A

152809932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461045-G-T

152809944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461033-A-G

152809957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84461020-A-G

http://identifiers.org/hco/4/GRCh38#152809980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84460998-C-A

152810179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84460903-A-G

152810212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84460875-T-C

152810231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84460853-T-G

152810267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84460817-A-G

152810279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84460805-T-A

152810289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84460795-A-G

152829481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455560-T-C

152829515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455526-G-A

152829515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455526-G-C

152829515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455526-G-T

152829616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455355-T-G

152829714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: synonymous variant
orthologous variants: 84455251-T-C

152829739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455226-T-C

152829739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455226-T-G

http://identifiers.org/hco/4/GRCh38#152829741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84455224-C-A

152829741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455224-C-T

152829744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455221-T-C

152829760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455205-A-G

152829924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84455115-A-G

152830233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84454331-G-A

http://identifiers.org/hco/4/GRCh38#152830336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84454266-C-A

152830336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84454266-C-T

152830490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84454124-A-G

152830786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84453562-T-G

152831162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84453147-A-G

152831196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84453117-A-G

152831238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84453078-A-G

http://identifiers.org/hco/4/GRCh38#152844571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84451027-C-A

152844571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84451027-C-T

152846930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84449915-T-G

152847849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84449137-C-T

152848282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84448771-T-C

152848342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84448714-G-A

152848342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84448714-G-T

152852714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446743-G-C

152852747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446704-A-T

152852790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84446666-C-T

152859833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84444910-A-G

152859833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84444910-A-T

152859964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84444767-T-C

152861208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443457-A-G

152861241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443423-C-G

152861323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443344-T-C

152861583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84443120-G-C

152861795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442673-G-A

152861795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442673-G-C

152861932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442562-T-C

152862016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442469-T-C

152862126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442375-C-T

152862136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442365-G-A

152862239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442250-A-G

152862260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442229-A-G

152863574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84442035-A-G

152863660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84441946-T-A

152863660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84441946-T-C

http://identifiers.org/hco/4/GRCh38#152863706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84441900-C-A

152863706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84441900-C-T

152863740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84441867-T-C

152865769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84439513-G-T

152868484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84438853-T-A

152868882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84438462-A-G

152868944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84438407-T-G

http://identifiers.org/hco/4/GRCh38#152869033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84438318-A-C

152869182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84438185-G-A

152869804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84437461-T-C

152870026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84437257-T-A

152870108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84437189-G-C

152870184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84437122-G-A

152870187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84437119-C-G

152870345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436951-A-T

152870523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436798-T-A

152870616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436705-A-G

http://identifiers.org/hco/4/GRCh38#152870634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84436687-C-A

152870634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436687-C-T

152870881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436461-T-C

http://identifiers.org/hco/4/GRCh38#152870890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84436452-C-A

152870890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436452-C-G

152871016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84436317-A-G

http://identifiers.org/hco/4/GRCh38#152872334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84435218-A-C

152872334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435218-A-T

152872339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435213-T-C

152872360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435199-T-A

152872360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435199-T-C

152872360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435199-T-G

152872381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435178-T-A

152872381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435178-T-C

152872425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435133-G-A

152872425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84435133-G-T

152872461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84435094-G-A

http://identifiers.org/hco/4/GRCh38#152872556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84434999-A-C

http://identifiers.org/hco/4/GRCh38#152872587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84434964-C-A

152872587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434964-C-T

http://identifiers.org/hco/4/GRCh38#152872591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84434960-C-A

152872591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434960-C-T

152872602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434949-T-A

152872602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434949-T-C

152872637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434915-A-G

http://identifiers.org/hco/4/GRCh38#152872643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84434875-C-A

152872683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434835-A-G

152872687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434744-T-A

152872687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434744-T-C

152873169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434129-A-G

152873182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84434116-C-G

152873398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84433919-A-G

http://identifiers.org/hco/4/GRCh38#152873821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84433199-A-C

152873821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84433199-A-G

152873873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84433152-A-G

152873873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84433152-A-T

152873880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84433145-C-T

152875437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84432614-G-T

152875471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84432560-G-C

152875508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84432528-C-G

152875543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84432493-T-C

152875730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84432331-G-A

152875730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84432331-G-T

152878348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84431665-T-C

152878353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84431660-C-T

152878399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84431642-C-T

152878451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84431592-T-G

152878571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84429222-G-C

152878586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84429210-C-G

152880811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427154-C-T

152880872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427106-T-G

152880879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427099-A-G

152880888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427083-T-C

152880889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427082-G-A

152880889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427082-G-T

152880946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84427026-G-A

152880969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 84427002-C-T

152881260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84426719-G-A

152881269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84426710-T-C

152881730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84424016-G-T

152881784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84423967-A-G

152881995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84423779-G-T

http://identifiers.org/hco/4/GRCh38#152882652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84423162-C-A

152882652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84423162-C-T

152882847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: missense variant
orthologous variants: 84422971-C-T

152882981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84422844-G-A

152882981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84422844-G-T

152883063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84422618-C-G

152883205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron variant
orthologous variants: 84422504-T-C

152883264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84422448-G-T

152883395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84422347-A-T

152884107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84421750-T-C

152886352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84419724-C-T

152887314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84418084-T-C

152887525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417893-G-A

152887939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417527-G-A

152888010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417388-A-G

152888010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417388-A-T

152888014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417384-G-T

152888015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417383-T-G

152888209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84417211-A-T

152888386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417035-G-A

152888386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84417035-G-T

152889002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84416550-G-A

152889026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84416529-A-G

152892791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84414314-T-G

152892898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84414208-G-C

152893058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84414053-A-G

152893059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84414052-T-C

152893102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84414010-A-G

http://identifiers.org/hco/4/GRCh38#152893433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84413792-A-C

152893433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84413792-A-G

152893433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84413792-A-T

152893837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84413338-A-G

152893846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84413329-C-G

152893867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84413308-T-G

152896749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412080-T-A

152896749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84412080-T-C

152896846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411983-T-C

152896942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411888-A-G

http://identifiers.org/hco/4/GRCh38#152897061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84411784-C-A

152897084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411759-G-A

152897196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411664-A-G

152897291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411584-G-A

152897296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411579-C-G

152897329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411560-T-A

152897355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411533-G-A

152897565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411262-G-A

152897602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411225-G-T

152897875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84411010-G-A

152898979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84410438-A-G

http://identifiers.org/hco/4/GRCh38#152899339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84410171-C-A

152899487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84410038-A-G

http://identifiers.org/hco/4/GRCh38#152900652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84409132-C-A

152900752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84409023-T-C

152900929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84408893-A-G

152901219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84408716-G-A

152901337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84408617-A-G

152901646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84408316-C-G

152903382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406480-A-T

152903413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406453-A-G

http://identifiers.org/hco/4/GRCh38#152903416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84406450-C-A

152903416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406450-C-T

152903435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406433-T-A

http://identifiers.org/hco/4/GRCh38#152903537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84406330-A-C

152903537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406330-A-G

152903792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406097-G-C

152903810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406079-A-G

152903825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84406069-G-A

http://identifiers.org/hco/4/GRCh38#152909706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84405577-C-A

152909865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405362-A-G

152909865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405362-A-T

152909914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405329-A-T

152909938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405306-G-A

152909938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405306-G-T

152909939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405305-G-A

152909939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405305-G-T

152909950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405294-G-A

152909950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405294-G-T

http://identifiers.org/hco/4/GRCh38#152909976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84405278-C-A

152909976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405278-C-G

152909988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405266-G-A

152909996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405258-A-G

152910007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84405245-T-A

152910083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84405177-A-G

152910289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 84404976-G-T

152910689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404558-G-T

http://identifiers.org/hco/4/GRCh38#152910710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84404539-C-A

152910710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404539-C-T

http://identifiers.org/hco/4/GRCh38#152910733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84404516-C-A

http://identifiers.org/hco/4/GRCh38#152910912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84404359-C-A

152911125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404132-T-C

152911153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404104-T-G

152911283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404007-G-A

152911283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404007-G-T

152911289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3 prime UTR variant
orthologous variants: 84404001-G-A

152911356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 84403935-A-G

152911425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 84403878-T-C

152911810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 84403493-T-A

152911866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 84403441-T-G

152911927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 84403381-C-G

152912069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84403249-A-G

152912072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84403246-G-A

http://identifiers.org/hco/4/GRCh38#152912101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84403218-C-A

152912131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84403186-A-G

152912268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84403050-G-A

152912313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84403010-A-G

152912317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84403006-G-T

http://identifiers.org/hco/4/GRCh38#152914140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#84399847-A-C

152914256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84399746-T-C

152914310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84399691-T-C

152916479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

152916479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

152916694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

152917249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84397153-C-T

152917390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84397070-G-T

152917668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84396818-C-T

152917695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84396796-G-C

152918086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84396294-A-G

152918181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21496
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84396202-T-G