42852723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118538968-T-G

http://identifiers.org/hco/9/GRCh38#42852756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118538893-C-A

42852756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118538893-C-G

42852756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118538893-C-T

42852819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118538830-G-T

42852910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538734-G-A

42852910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118538734-G-T

42870946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529797-T-C

42871005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118529736-G-A

42871005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118529736-G-T

42871040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118529698-T-A

42871040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118529698-T-C

42871064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529661-T-C

42871099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529623-T-A

42871099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529623-T-C

42871099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529623-T-G

42871117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529605-G-A

42871117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529605-G-T

42871134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529595-A-G

42871136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529593-G-A

42871166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529563-T-C

42873560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688297-T-C

42873571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688312-T-C

42873579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688320-A-G

http://identifiers.org/hco/9/GRCh38#42873602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#14688340-C-A

42873602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688340-C-T

42873604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688342-G-T

42873608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688346-T-A

42873608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688346-T-C

42873617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688355-A-T

42873656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

42873688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688376-T-A

42873729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 14688412-A-G

42873730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 14688413-T-A

42873891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688564-T-C

42873910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688576-G-T

42874010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14689264-A-G

42874043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14689297-A-T

42874240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528523-A-G

42874288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528482-G-C

42874314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528457-G-T

42874327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528444-T-A

42874362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528408-A-T

42879210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518131-G-A

42879233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518112-A-G

http://identifiers.org/hco/9/GRCh38#42879286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118518064-C-A

42879286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518064-C-T

42879294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518056-A-G

http://identifiers.org/hco/9/GRCh38#42879350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118518001-A-C

42879350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518001-A-G

42879350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518001-A-T

42879425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517943-G-C

42879425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517943-G-T

42879426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517942-G-C

42879504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517889-A-G

http://identifiers.org/hco/9/GRCh38#42879532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517857-C-A

http://identifiers.org/hco/9/GRCh38#42879536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118517853-A-C

42879593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517801-G-A

42879601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517793-G-A

42879601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517793-G-C

42880206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517231-C-T

42880212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517225-G-T

42880292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517149-G-T

42880487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516955-A-T

42880539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516924-A-G

42880546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516917-A-G

42880546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516917-A-T

42880624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118516840-T-C

42880695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516773-A-G

42880695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516773-A-T

42880701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516767-T-C

42880701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516767-T-G

42880728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516745-T-A

42880728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516745-T-C

42880803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118516664-T-C

42880824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 118516643-T-C

42880852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516615-A-G

42880852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516615-A-T

42880854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516613-A-G

42880854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516613-A-T

42880879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118516591-T-C

http://identifiers.org/hco/9/GRCh38#42880927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118516541-A-C

http://identifiers.org/hco/9/GRCh38#42882099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118515141-A-C

42882133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118515107-T-A

42882203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118515050-A-G

42883035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513796-T-A

42883060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513771-G-C

42883060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513771-G-T

42883108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513731-T-C

42883118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513724-C-G

42883118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513724-C-T

42883193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513651-T-C

42883364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513479-A-G

42883364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513479-A-T

42883450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513413-C-G

http://identifiers.org/hco/9/GRCh38#42884900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118513182-A-C

42884900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513182-A-G

42884900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513182-A-T

http://identifiers.org/hco/9/GRCh38#42885075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118513073-C-A

42885076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513072-C-T

42885167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513042-A-G

42885167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118513042-A-T

http://identifiers.org/hco/9/GRCh38#42885436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512961-C-A

42885439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512958-A-G

42885487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512906-T-G

42885512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512879-C-T

42885596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512823-C-T

http://identifiers.org/hco/9/GRCh38#42885627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512802-C-A

42885681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512768-G-T

http://identifiers.org/hco/9/GRCh38#42885780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512669-C-A

42885827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512622-A-G

42885865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512585-G-A

42886516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512350-G-A

42886518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512348-G-A

42886543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512325-A-G

42886564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512304-T-G

http://identifiers.org/hco/9/GRCh38#42886586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512286-A-C

42886586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512286-A-T

42886610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512262-G-A

42886637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512234-A-G

42886637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512234-A-T

42886648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512215-A-G

http://identifiers.org/hco/9/GRCh38#42886650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512213-C-A

42886650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512213-C-T

http://identifiers.org/hco/9/GRCh38#42886686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512185-C-A

42886686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512185-C-T

http://identifiers.org/hco/9/GRCh38#42886746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118512134-C-A

42886746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512134-C-T

42886807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512079-G-A

42886807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512079-G-C

42886826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512060-G-A

42886826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512060-G-T

42886829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512057-G-A

42886829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512057-G-T

42886845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118512041-A-G

42886858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118512028-A-T

http://identifiers.org/hco/9/GRCh38#42887517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511566-C-A

42887517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511566-C-T

42887532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511551-G-T

http://identifiers.org/hco/9/GRCh38#42887610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511491-A-C

42887610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511491-A-T

42887677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511428-G-T

http://identifiers.org/hco/9/GRCh38#42887688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511417-C-A

42887688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511417-C-G

42887688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511417-C-T

42887764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511341-A-G

http://identifiers.org/hco/9/GRCh38#42887784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511319-A-C

42887842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511267-A-T

42887850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511259-C-T

42887875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511236-G-T

42887952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511164-G-A

42887962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511160-G-A

http://identifiers.org/hco/9/GRCh38#42888013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118511115-C-A

42888013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511115-C-G

42888040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511075-C-T

42888054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511061-A-G

42891974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503777-T-C

http://identifiers.org/hco/9/GRCh38#42892202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118503128-A-C

42892236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503094-T-G

42892281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503049-T-A

42892394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502983-G-A

42892394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502983-G-C

42892394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502983-G-T

42892471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502889-G-A

42892471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502889-G-T

http://identifiers.org/hco/9/GRCh38#42892513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118502847-A-C

42892513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502847-A-G

42892529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-T-A

42892529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-T-C

42892529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502831-T-G

http://identifiers.org/hco/9/GRCh38#42892544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118502816-A-C

42892544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502816-A-G

42892544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502816-A-T

42892545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502815-T-A

42892545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502815-T-C

42892569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502791-G-T

42892570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502790-A-G

42892594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502766-G-A

42892594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118502766-G-C

42892717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502635-G-A

42892717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502635-G-C

42892717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502635-G-T

http://identifiers.org/hco/9/GRCh38#42892742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118502610-A-C

42892742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502610-A-G

42893449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501204-G-T

42893672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500997-T-G

42893725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500955-G-A

42893725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500955-G-C

42893774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500906-G-A

42893774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500906-G-T

42893864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500823-T-C

42893899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500788-G-A

42893899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500788-G-T

42894033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500654-G-A

42894106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500581-G-A

42894106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500581-G-T

42894148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500539-G-C

http://identifiers.org/hco/9/GRCh38#42894244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118500443-A-C

42894244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500443-A-G

42894281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500400-C-G

42894281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500400-C-T

42894361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500320-G-A

42894361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500320-G-T

42894373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500308-A-G

42894373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500308-A-T

42894376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500305-A-G

42894415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500264-T-C

42894479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500200-G-A

42894479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500200-G-T

42894557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500122-G-A

42894557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500122-G-C

42894557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500122-G-T

42894596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500083-G-A

42894596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118500083-G-C

42894662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118499990-G-A

42894662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118499990-G-C

42894662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non coding transcript exon variant
orthologous variants: 118499990-G-T

http://identifiers.org/hco/9/GRCh38#42894677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499975-A-C

42894677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499975-A-G

42894728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499924-T-C

42894737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499915-G-A

42894737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499915-G-C

42894737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499915-G-T

42894743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499909-G-A

42894743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118499909-G-T

http://identifiers.org/hco/9/GRCh38#42894763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118499889-C-A

42894763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118499889-C-G

42896331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118498922-G-A

http://identifiers.org/hco/9/GRCh38#42896548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118498692-A-C

42896548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498692-A-G

http://identifiers.org/hco/9/GRCh38#42896725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118498382-C-A

42896725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498382-C-T

42896847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498289-G-A

42897011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497960-C-G

42897073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497899-C-T

42897291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497539-C-G

42897303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497527-C-T

42897362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497477-T-C

42897442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497426-A-G

http://identifiers.org/hco/9/GRCh38#42897476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118497399-C-A

http://identifiers.org/hco/9/GRCh38#42897591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118497314-C-A

42897591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497314-C-T

42897813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118497116-A-G

42901256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14718208-G-A

42901368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14718320-T-C

http://identifiers.org/hco/9/GRCh38#42901381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#14718333-C-A

42901381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14718333-C-T

42901389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14718341-T-C

http://identifiers.org/hco/9/GRCh38#42901459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#14718402-A-C

42901459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14718402-A-G

42902333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489990-T-G

42902398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489878-C-T

http://identifiers.org/hco/9/GRCh38#42902435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118489841-A-C

42902435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489841-A-T

42902441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489837-G-C

42902450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489828-T-C

42902450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489828-T-G

42902451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489827-C-T

42902511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489770-C-G

http://identifiers.org/hco/9/GRCh38#42902576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118489704-A-C

42902576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489704-A-G

42902632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489660-C-G

42902688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489576-A-G

42902709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489555-C-T

42902720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489544-T-A

42902734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489530-A-G

42902734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118489530-A-T

42903118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488986-C-T

42903144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488959-A-G

42903193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488913-A-G

42903220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488880-T-C

42903251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488744-G-T

http://identifiers.org/hco/9/GRCh38#42903431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118488566-C-A

http://identifiers.org/hco/9/GRCh38#42903512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118488471-C-A

42903512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488471-C-G

42903512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118488471-C-T

42905626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487913-T-C

42905665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487882-G-A

42905841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487736-T-C

42905851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487725-T-A

42905851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487725-T-C

42905897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487675-C-T

http://identifiers.org/hco/9/GRCh38#42905956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487614-C-A

http://identifiers.org/hco/9/GRCh38#42905963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487607-C-A

42905963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487607-C-G

42905963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487607-C-T

42906045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487532-T-C

http://identifiers.org/hco/9/GRCh38#42906051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487526-C-A

42906115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487467-C-T

42906206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487384-T-C

42906274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487278-T-G

http://identifiers.org/hco/9/GRCh38#42906329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487230-C-A

http://identifiers.org/hco/9/GRCh38#42906340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118487219-C-A

42906340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118487219-C-T

42906571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486998-C-T

42906705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486855-T-C

42906713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486847-A-G

42910637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485835-T-C

http://identifiers.org/hco/9/GRCh38#42910640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118485832-C-A

42910640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485832-C-T

42910645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485827-A-G

42910699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485775-T-A

42910819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118485652-T-C

http://identifiers.org/hco/9/GRCh38#42910918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118485553-A-C

42911054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485426-T-A

42911076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485404-A-G

42911134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485306-T-C

42911151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485289-A-T

42911557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484856-A-G

42911579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484833-A-G

42911579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484833-A-T

42911591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484821-T-C

42911624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118484791-A-G

42911624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118484791-A-T

42911705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118484707-C-G

42911705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118484707-C-T

42911793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118484619-T-A

42911793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118484619-T-C

42911816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 118484596-G-A

42911816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 118484596-G-T

42911820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484592-G-A

42911876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484541-T-C

http://identifiers.org/hco/9/GRCh38#42911912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484518-A-C

42911912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484518-A-G

42911952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484498-G-A

42911952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484498-G-C

42911952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484498-G-T

42912098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484420-T-G

http://identifiers.org/hco/9/GRCh38#42912215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118484286-A-C

42912215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484286-A-G

42912261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484214-A-G

42912274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484201-G-C

http://identifiers.org/hco/9/GRCh38#42913327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483952-A-C

http://identifiers.org/hco/9/GRCh38#42913337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483942-A-C

42913391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483896-G-C

42913441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483847-G-T

42913524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483768-A-T

42913545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483747-G-A

42913609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483687-C-T

42913645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483653-G-C

http://identifiers.org/hco/9/GRCh38#42913672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483625-C-A

42913753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483544-G-A

42913753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483544-G-C

42913753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483544-G-T

http://identifiers.org/hco/9/GRCh38#42913761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483536-C-A

42913777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483520-G-A

42913777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483520-G-T

http://identifiers.org/hco/9/GRCh38#42913907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#118483387-C-A

42913907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483387-C-T

42913909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118483385-A-G

42913986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483318-T-C

42914077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483234-G-A

42914077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118483234-G-T

42914263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483079-T-C

42914289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483053-C-T

42919688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118479364-T-C

42919725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479323-G-A

42919725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479323-G-C

42919725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479323-G-T

42919753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479296-G-A

42919753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479296-G-T

42919785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479272-A-G

42919810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479241-T-A

42919810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479241-T-C

42919830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118479224-T-C