111483477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607887-G-A

111483477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607887-G-C

111483477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607887-G-T

111483482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607882-G-A

111483482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607882-G-T

111483587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607828-G-A

111483587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 39607828-G-T

111483695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39607702-G-A

http://identifiers.org/hco/6/GRCh38#111483724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39607673-C-A

http://identifiers.org/hco/6/GRCh38#111483725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39607672-C-A

111483725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607672-C-T

http://identifiers.org/hco/6/GRCh38#111483738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39607659-A-C

111483738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607659-A-G

111483738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607659-A-T

111483749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607648-G-A

111483749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607648-G-C

111483749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607648-G-T

111483762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607635-C-T

111483885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607505-T-A

111483885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607505-T-C

111483911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607454-G-A

111483911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607454-G-T

111484057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607300-C-T

http://identifiers.org/hco/6/GRCh38#111484088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39607257-C-A

111484090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607255-T-A

111484090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607255-T-G

111484123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39607218-G-T

111484169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39607162-G-T

111484211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39607125-G-A

111484211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39607125-G-T

111484256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39607078-T-C

111484454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606901-C-T

111484532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606824-T-G

http://identifiers.org/hco/6/GRCh38#111484652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39606716-C-A

111484652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39606716-C-G

111484734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39606632-T-G

111484738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 39606628-A-T

http://identifiers.org/hco/6/GRCh38#111484742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39606624-A-C

111485000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606400-A-G

111485082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606322-A-G

111485133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606232-A-G

111485143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606222-C-T

111486913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39605059-T-C

111487190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39604818-T-C

111487222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39604788-T-G

111487790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39604117-G-A

111487790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39604117-G-T

111488054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39603872-T-C

http://identifiers.org/hco/6/GRCh38#111492136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39601264-A-C

111494423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39597730-G-T

http://identifiers.org/hco/6/GRCh38#111494928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39597699-C-A

111494928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39597699-C-T

111494943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39597684-A-G

http://identifiers.org/hco/6/GRCh38#111494970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39597654-C-A

111494970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39597654-C-T

111494985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39597639-T-G

111495017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597605-G-A

111495017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597605-G-T

111495049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597573-G-A

111495080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597543-C-T

111495090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597533-G-A

111495102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597521-G-A

111495287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597316-A-G

http://identifiers.org/hco/6/GRCh38#111495399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39597202-C-A

111495414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597187-T-C

111495415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597186-G-C

111495415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597186-G-T

111495418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597183-C-G

111495438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597163-T-C

111495513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39597100-T-C

http://identifiers.org/hco/6/GRCh38#111495689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39596945-C-A

111495728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39596907-G-T

111495803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39596835-G-A

111495990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39596054-C-T

111496540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39595568-T-C

111496588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39595520-T-A

111496781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39595329-A-G

111497498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39594092-G-A

http://identifiers.org/hco/6/GRCh38#111499784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39592271-C-A

111499784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39592271-C-T

111499840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39592227-G-A

111500085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39591857-A-T

111500218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39591750-A-G

111500722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39589648-G-A

111501972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39588566-T-A

111502183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39588359-G-C

111503197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39587361-T-C

111503351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39587205-C-T

111503355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39587201-G-A

111503401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39587158-G-T

111503565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39587001-G-A

111503565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39587001-G-T

111504305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39586131-G-A

111504377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39586043-C-T

111505172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39585399-T-G

111508960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39583686-T-G

111509066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39583543-C-G

111509067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39583542-C-T

111509188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39583421-T-C

111510107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39582511-A-G

http://identifiers.org/hco/6/GRCh38#111513908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39579884-C-A

111513908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579884-C-T

111514318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579393-G-A

111514348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579363-C-T

111514350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579361-G-A

111514350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579361-G-T

111514421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579290-G-A

111515311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39579033-T-C

http://identifiers.org/hco/6/GRCh38#111515723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39577861-C-A

http://identifiers.org/hco/6/GRCh38#111515814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39577771-A-C

111516265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39577216-A-G

111516475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39576994-C-T

111516612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39576862-T-G

111517311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39576089-G-A

111517663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39575749-T-A

111517816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39575607-G-A

111518171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39575264-A-T

http://identifiers.org/hco/6/GRCh38#111518263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39574332-C-A

111518468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39574134-A-G

111518473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39574129-C-T

111518988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39573251-T-A

111518998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39573241-T-C

111519361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39573192-G-A

http://identifiers.org/hco/6/GRCh38#111519378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39573175-C-A

111519378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39573175-C-T

111523867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39568981-T-C

111523867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39568981-T-G

111524014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39568837-G-A

111524289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39568573-T-G

111524702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39568308-C-T

111524814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39568212-T-C

http://identifiers.org/hco/6/GRCh38#111524892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39568145-C-A

111524996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39567998-T-C

111525265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39567764-G-A

111525575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39567445-A-G

http://identifiers.org/hco/6/GRCh38#111525651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39567367-A-C

http://identifiers.org/hco/6/GRCh38#111529054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39564159-A-C

111529054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39564159-A-T

111529102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39564111-G-A

111529233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39563983-C-T

111529249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39563972-G-A

111529398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39563857-C-G

111530378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39563344-C-G

111531295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39562571-G-A

111531719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39561824-A-G

111531791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39561562-C-T

111531868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39561445-G-A

111531900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39561413-T-C

111532428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39560945-A-G

111533137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39560262-A-G

111533139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39560260-A-G

111533235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39560177-C-T

http://identifiers.org/hco/6/GRCh38#111533625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39559636-C-A

111533625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559636-C-G

111533732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559562-T-C

111533738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559561-C-T

111533743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559556-A-G

http://identifiers.org/hco/6/GRCh38#111533970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39559352-A-C

111534068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559258-T-C

111534151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559178-C-T

111534347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39559014-G-A

http://identifiers.org/hco/6/GRCh38#111534381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39558980-C-A

111534524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39558845-A-G

111534923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39558434-T-G

111534952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39558371-A-T

111535454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39557663-T-C

111535510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39557619-A-G

111535530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39557601-T-C

111537336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39551736-A-G

111537388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39551687-G-C

111537536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39551620-A-T

111537726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39551469-C-T

111537837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39551359-G-A

111538348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39550856-C-T

111538513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39550718-A-G

111539360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39550356-A-G

111539490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39550231-T-C

111539612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39550133-C-G

111539758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549999-C-T

111539978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549781-G-A

111539978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549781-G-T

111540484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549443-C-T

111540544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549383-T-G

111540591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549347-T-A

111540592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549346-T-A

111540665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549300-T-C

111540783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39549176-T-C

111541311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39548691-C-T

111541471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39548531-G-C

111541781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39548266-T-C

111542328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39547573-C-G

111542328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39547573-C-T

http://identifiers.org/hco/6/GRCh38#111542668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39547328-C-A

111543962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39547269-A-G

111544032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39547195-A-T

111544094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39547133-G-C

111544417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39546832-T-C

111544773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39546377-T-G

111544804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39546347-T-G

111544900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39546249-C-T

http://identifiers.org/hco/6/GRCh38#111544962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39546169-A-C

111544962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39546169-A-T

111545207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39545782-T-C

111545316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39545669-C-T

111545391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39545560-C-T

111548707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39542189-T-G

111549045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39541419-G-A

111549413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39541065-G-C

111550123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39540359-G-A

111550147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39540334-G-A

111550828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39537053-C-G

111550883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39536990-G-A

111551191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39536839-C-T

111551266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39536799-G-C

http://identifiers.org/hco/6/GRCh38#111551362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39536703-C-A

111551362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39536703-C-T

111551397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39536670-C-G

111551781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39536307-C-T

111552823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39535280-G-T

http://identifiers.org/hco/6/GRCh38#111552972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39535142-A-C

111554468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39534608-T-C

111554487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39534589-G-C

111554522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39534554-G-T

111554574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39534502-G-A

http://identifiers.org/hco/6/GRCh38#111555342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39533820-A-C

111555418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39533745-G-A

111555499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39533675-C-T

111556360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39533111-G-A

111556666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39532815-T-C

111557922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39531737-A-G

111557922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39531737-A-T

http://identifiers.org/hco/6/GRCh38#111557934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39531725-C-A

http://identifiers.org/hco/6/GRCh38#111558680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39531062-C-A

111558680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39531062-C-T

111558700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39531036-G-A

111558749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530994-G-T

111558870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530882-G-C

111559072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530696-G-A

111559072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530696-G-C

111559072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530696-G-T

http://identifiers.org/hco/6/GRCh38#111559091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39530679-C-A

111559132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530638-A-G

111559251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530622-G-A

111559251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530622-G-T

111559445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530483-G-A

111559466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530462-T-C

111559468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39530460-T-C

http://identifiers.org/hco/6/GRCh38#111559646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39530284-A-C

111559689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39530244-T-C

111559729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39530205-T-C

111559730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39530204-C-T

111559925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39530011-A-G

111562208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39527718-A-G

111562218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39527708-G-T

111562440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39527183-G-A

http://identifiers.org/hco/6/GRCh38#111562904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39527049-C-A

http://identifiers.org/hco/6/GRCh38#111562922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39527020-C-A

111562928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39527014-A-G

111563055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39526885-T-C

111563081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39526860-G-T

111563148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39526797-T-A

http://identifiers.org/hco/6/GRCh38#111563478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39525557-A-C

111563478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39525557-A-G

111563492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39525543-A-T

111563534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39525501-G-A

111563538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39525494-C-T

111564475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39524705-T-A

111564498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39524678-G-A

111564618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39524614-G-T

111564654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39524585-A-G

111564654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39524585-A-T

111564882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39524365-C-T

http://identifiers.org/hco/6/GRCh38#111565197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39524079-A-C

111565268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39524009-T-A

111565268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39524009-T-C

111565624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39523710-C-T

111565663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39523671-C-G

111566170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39523186-C-T

http://identifiers.org/hco/6/GRCh38#111566318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39523068-A-C

111566344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39523043-A-T

111566639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522724-A-G

111566640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522723-G-A

111566640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522723-G-T

111566659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522704-T-C

http://identifiers.org/hco/6/GRCh38#111566673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39522690-C-A

http://identifiers.org/hco/6/GRCh38#111566680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39522683-C-A

111566680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522683-C-G

111566680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522683-C-T

http://identifiers.org/hco/6/GRCh38#111566681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39522682-C-A

111566681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522682-C-G

111566681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522682-C-T

111566879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522507-T-C

http://identifiers.org/hco/6/GRCh38#111566900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39522489-C-A

111566900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522489-C-T

111566973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39522415-A-G

http://identifiers.org/hco/6/GRCh38#111567007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39522381-C-A

111567007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522381-C-G

111567007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522381-C-T

http://identifiers.org/hco/6/GRCh38#111567027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39522361-A-C

111567027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522361-A-G

111567335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522058-T-C

111567335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522058-T-G

111567342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522051-T-A

111567342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522051-T-C

111567342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39522051-T-G

111567416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521977-C-T

111567485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521908-T-C

http://identifiers.org/hco/6/GRCh38#111567693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39521701-C-A

111567693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 39521701-C-T

111567708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521687-T-A

111567796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521603-A-G

111567820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521579-G-A

111567820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521579-G-T

http://identifiers.org/hco/6/GRCh38#111567821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39521578-C-A

111567821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521578-C-T

111567827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521572-G-A

111567827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521572-G-T

111568209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521239-G-A

111568472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521080-T-C

111568473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521079-G-A

111568489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39521063-G-A

111570726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39518751-A-G

111571539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39518692-G-A

111571865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39518442-A-G

111571981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39518374-A-G

111572204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39518088-T-G

111572394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517912-G-A

111572394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517912-G-C

111572394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517912-G-T

111572471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517843-A-G

111572570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517751-G-A

111572572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517749-A-T

111572633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517691-G-A

111572633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517691-G-T

111572636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517688-G-A

111572636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39517688-G-T

111572721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517562-T-G

111572740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517543-T-G

111572846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517439-A-G

111572846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517439-A-T

111572864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517421-G-A

111572864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517421-G-T

111572872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39517411-A-G

111573031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517253-T-C

111573126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517179-T-A

111573126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517179-T-C

111573285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39517015-C-T

111573533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516776-G-T

http://identifiers.org/hco/6/GRCh38#111573534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39516775-C-A

111573534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516775-C-T

111573571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516739-A-G

111573645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516667-T-C

111573659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516657-G-T

111573686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516630-T-A

111573719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516596-G-T

111573748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516563-A-G

111573866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516452-G-A

111573866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516452-G-C

111573914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39516392-A-T

111574223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39516118-T-C

111574370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39516006-A-G

111574456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39515921-A-G

http://identifiers.org/hco/6/GRCh38#111574470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39515907-C-A

111574768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39515591-T-A

http://identifiers.org/hco/6/GRCh38#111574797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39515563-C-A

111574823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39515537-A-G

111574823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39515537-A-T

111574836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39515525-G-T

http://identifiers.org/hco/6/GRCh38#111575786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39515249-C-A

111575786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39515249-C-G

111575786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39515249-C-T

http://identifiers.org/hco/6/GRCh38#111575841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39515194-C-A

111575841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39515194-C-G

111575841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39515194-C-T

111575864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39515169-A-G

http://identifiers.org/hco/6/GRCh38#111575934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39515100-C-A

111577325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39511788-C-T

111578044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39511696-T-C

http://identifiers.org/hco/6/GRCh38#111578131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39511618-C-A

111578131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39511618-C-T

111580160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510767-G-T

111580178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510749-T-C

http://identifiers.org/hco/6/GRCh38#111580434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39510494-C-A

111580435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510493-T-C

http://identifiers.org/hco/6/GRCh38#111580440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39510488-C-A

111580440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510488-C-G

111580440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510488-C-T

111580500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510429-A-G

111580985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39510030-C-G

111581364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39509552-T-C

111582141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39509154-C-T

111582249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39509048-C-G

111582561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508736-G-A

111582592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508708-T-G

111582679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508632-C-T

111582698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508614-C-T

111582911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508412-C-G

111583001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508334-C-G

111583037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39508304-A-G

111584461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39507540-G-C

111584489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39507512-G-A

111584747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39507209-A-G

111585004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39507018-G-A

111585111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39506926-A-G

111585356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39506676-C-T

111585395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39506632-G-A

111586063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39505961-G-A

111587102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39504941-T-C

111587591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39504798-A-G

111587675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39504714-A-G

111587770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39504618-A-G

111590935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39502937-A-G

111591151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39502742-C-T

111591166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502727-A-T

111591306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502602-A-G

http://identifiers.org/hco/6/GRCh38#111591334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39502574-C-A

111591334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502574-C-T

http://identifiers.org/hco/6/GRCh38#111591422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39502483-C-A

http://identifiers.org/hco/6/GRCh38#111591624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#39502269-C-A

111591635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502258-T-G

111591684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502209-C-T

111591719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502174-C-T

111591758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502141-C-G

111591788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502111-G-C

111591818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39502081-T-C

111592066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 39501872-C-T

111592500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39501424-T-G

111592711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39501256-T-C

111593064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39500948-T-G

http://identifiers.org/hco/6/GRCh38#111593102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39500913-C-A

111593102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39500913-C-T

111593110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39500905-A-T

http://identifiers.org/hco/6/GRCh38#111593621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39500339-C-A

111593621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39500339-C-T

111593626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39500334-C-G

111595321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39499655-C-G

111595377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39499596-A-G

111597824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39498735-C-T

111597883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498671-T-A

111597883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498671-T-G

111597892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498662-T-A

http://identifiers.org/hco/6/GRCh38#111597902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39498652-C-A

111597902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498652-C-G

111597902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498652-C-T

http://identifiers.org/hco/6/GRCh38#111597986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39498569-C-A

http://identifiers.org/hco/6/GRCh38#111597999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39498557-C-A

111597999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498557-C-T

111598018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498538-G-A

111598018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498538-G-T

111598029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498529-G-A

111598029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498529-G-T

http://identifiers.org/hco/6/GRCh38#111598142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39498362-C-A

111598142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498362-C-G

111598142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498362-C-T

111598144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498360-G-T

111598366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498172-T-C

111598425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498132-A-T

111598471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39498099-A-G

http://identifiers.org/hco/6/GRCh38#111598809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39497840-A-C

111598851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39497797-G-A

111598851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39497797-G-T

111599011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39497646-C-T

111599013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39497644-C-T

111599388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39497127-C-T

111599683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39496866-C-T

http://identifiers.org/hco/6/GRCh38#111599780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#39496773-C-A

111599865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39496641-G-T

111600313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39496316-G-A

111600571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39496088-T-C

111601081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39494708-T-C