http://identifiers.org/hco/10/GRCh38#11850667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6122044-C-A

11850754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121980-A-G

11850832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121905-G-T

11850901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121838-G-A

11850901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121838-G-C

11850928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121810-G-A

11850928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121810-G-T

11851413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121106-T-C

http://identifiers.org/hco/10/GRCh38#11851436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6121088-A-C

11851436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121088-A-G

http://identifiers.org/hco/10/GRCh38#11851457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6121074-C-A

11851457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121074-C-T

11851488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6121051-A-T

11851568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120954-A-G

11851594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120928-A-G

11851647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120872-G-T

11851648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120871-G-A

11851697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120823-G-A

11851697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120823-G-C

11851697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120823-G-T

11851733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120767-G-A

11851733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120767-G-C

11851733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6120767-G-T

11851767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6120730-A-G

11852031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6118885-C-T

11852113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6118804-C-T

11852193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6118724-C-T

11852220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118697-G-A

http://identifiers.org/hco/10/GRCh38#11852344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6118616-C-A

11852344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118616-C-G

11852355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118605-G-A

11852355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118605-G-T

11852509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118473-C-G

11852509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118473-C-T

11852552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6118433-G-T

11856392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117994-G-A

11856392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117994-G-C

11856412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117974-G-A

11856527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117858-C-T

http://identifiers.org/hco/10/GRCh38#11856541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6117844-A-C

11856651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117735-C-G

http://identifiers.org/hco/10/GRCh38#11856724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6117673-C-A

11856724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117673-C-T

11856780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117659-A-G

11856996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6117487-C-T

11857290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6117194-C-T

http://identifiers.org/hco/10/GRCh38#11866345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6108057-C-A

11866345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6108057-C-T

11866449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6107932-T-A

11866502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6107887-C-G

11866502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6107887-C-T

11866612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6107793-G-A

11866723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6107682-G-C

11866723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6107682-G-T

11866736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6107669-C-G

11868063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106915-A-G

11868091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106888-T-C

http://identifiers.org/hco/10/GRCh38#11868103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106879-A-C

11868103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106879-A-T

11868207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106776-C-T

11868221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106762-C-T

11868247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106737-A-G

11868332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106628-A-G

11868413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106561-C-T

11868431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106543-A-T

11869204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106450-G-A

11869219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106435-G-A

11869219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106435-G-T

http://identifiers.org/hco/10/GRCh38#11869264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106388-C-A

11869264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106388-C-T

11869271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106374-A-G

11869271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106374-A-T

11869297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106346-G-T

http://identifiers.org/hco/10/GRCh38#11869335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106311-C-A

11869335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106311-C-G

11869346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6106300-G-T

11869392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106261-G-A

11869392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106261-G-T

http://identifiers.org/hco/10/GRCh38#11869413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106243-C-A

11869413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106243-C-G

11869413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6106243-C-T

11869485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6106174-T-C

11869490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 6106169-G-T

11869578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6106060-G-A

11869578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6106060-G-T

http://identifiers.org/hco/10/GRCh38#11869579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106059-C-A

11869579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6106059-C-T

http://identifiers.org/hco/10/GRCh38#11869597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6106041-A-C

11869666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105969-T-C

http://identifiers.org/hco/10/GRCh38#11869737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105898-C-A

11869737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105898-C-T

http://identifiers.org/hco/10/GRCh38#11869744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105891-C-A

11869744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105891-C-G

11869744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105891-C-T

11869777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105858-A-G

11869793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105842-G-A

11869793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105842-G-C

11869793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105842-G-T

http://identifiers.org/hco/10/GRCh38#11869801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105834-A-C

11869801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105834-A-G

11869801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105834-A-T

11869814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105818-G-A

11869814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105818-G-T

11869870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105756-A-G

11869870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105756-A-T

11870011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105600-G-A

11870011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105600-G-T

11870067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105528-G-A

11870067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105528-G-C

11870067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105528-G-T

11870069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105526-G-A

11870069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105526-G-C

11870069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105526-G-T

http://identifiers.org/hco/10/GRCh38#11870070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105525-C-A

11870070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105525-C-G

11870070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105525-C-T

http://identifiers.org/hco/10/GRCh38#11870071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105524-C-A

11870071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105524-C-T

11870106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105477-G-A

11870106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105477-G-C

11870106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105477-G-T

http://identifiers.org/hco/10/GRCh38#11870113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105465-C-A

11870113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105465-C-G

11870113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105465-C-T

http://identifiers.org/hco/10/GRCh38#11870114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105464-C-A

11870114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105464-C-G

11870114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105464-C-T

11870201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105377-T-C

11870227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105351-A-G

http://identifiers.org/hco/10/GRCh38#11870236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105342-C-A

11870236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105342-C-T

http://identifiers.org/hco/10/GRCh38#11870266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105303-A-C

11870266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105303-A-G

11870296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105270-T-C

11870414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105137-G-A

11870414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105137-G-C

11870414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105137-G-T

http://identifiers.org/hco/10/GRCh38#11870431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6105105-C-A

11870431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105105-C-G

11870431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6105105-C-T

http://identifiers.org/hco/10/GRCh38#11870591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6104972-C-A

11870591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104972-C-T

11870597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104966-C-G

11870597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104966-C-T

11870829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104866-T-C

11870897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104773-G-A

11870897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104773-G-T

11870932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104741-T-C

11871053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104591-A-G

http://identifiers.org/hco/10/GRCh38#11871087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6104562-C-A

11871087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104562-C-T

11871088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104561-G-A

11871088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104561-G-T

11871098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104552-G-A

11871100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104550-T-C

11871100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104550-T-G

11871249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104395-G-T

11871299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104357-C-T

11871385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104303-C-T

http://identifiers.org/hco/10/GRCh38#11871557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6104139-C-A

11871665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6104037-C-T

11871850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6103848-G-C

http://identifiers.org/hco/10/GRCh38#11871862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6103836-C-A

11872029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6103680-T-C

11872208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6103531-G-A

11872313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103445-G-C

11872551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6103246-G-C

11873130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102937-A-T

11873168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102901-C-T

11873231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102832-G-A

11873245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102818-G-A

http://identifiers.org/hco/10/GRCh38#11874562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6102227-C-A

11874562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6102227-C-T

11874593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102197-T-A

11874593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102197-T-C

11874651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102149-G-A

11874651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102149-G-T

11874662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102139-G-A

11874662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102139-G-T

11874798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102003-G-T

11874800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6102001-T-C

11874840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6101961-G-C

11874909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6101888-G-A

11874909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6101888-G-T

11874927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6101873-G-A

11875000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6101815-T-C

11875001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6101814-G-C

11875939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6094054-G-A

11875999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6093997-C-G

11875999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6093997-C-T

11876052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6093915-G-C

11876118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6093863-G-A

11876342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6093632-G-C

11876342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6093632-G-T

11876536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6093499-A-T

11877693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6091949-C-T

11877890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6091828-G-A

11877896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6091822-G-C

11877904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6091814-G-A

http://identifiers.org/hco/10/GRCh38#11877921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6091797-C-A

http://identifiers.org/hco/10/GRCh38#11878066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6091650-C-A

11880365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6090471-C-T

http://identifiers.org/hco/10/GRCh38#11882263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#6088693-C-A

11882388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6088571-G-C

11882644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6088191-C-G

11882644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6088191-C-T

11882671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6088152-C-T

11882693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6088130-C-G

11882869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087976-G-T

11882891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087951-T-C

11883063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087556-G-A

http://identifiers.org/hco/10/GRCh38#11883082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6087537-C-A

11883104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087512-G-A

11883140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087479-T-C

11883143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6087476-G-A

11886205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6086052-G-A

http://identifiers.org/hco/10/GRCh38#11886270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#6085990-C-A

11886431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085851-C-G

11886431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085851-C-T

11886435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085847-G-C

11886435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085847-G-T

11886565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085734-G-A

11886635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085672-G-C

11886676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085631-C-G

11886676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085631-C-T

11886714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27343
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6085591-G-A