http://identifiers.org/hco/3/GRCh38#19879829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53706174-C-A

19879829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53706174-C-G

19882412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53706918-G-A

19882412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53706918-G-T

19882423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53706929-A-G

19882423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53706929-A-T

19882565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 53707789-G-A

19882565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 53707789-G-C

19882565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 53707789-G-T

19882735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53707959-G-T

19882789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708009-T-C

19882789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708009-T-G

http://identifiers.org/hco/3/GRCh38#19882796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53708016-C-A

19882830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708050-G-T

19882859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708072-G-A

19882859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708072-G-T

http://identifiers.org/hco/3/GRCh38#19884263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53708310-C-A

19884263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708310-C-T

19884322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708366-G-A

19884322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708366-G-T

19884336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708382-G-T

19884431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53708491-A-G

19884440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53708500-A-G

19884554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53708614-G-A

19884554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53708614-G-T

19884583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53708643-C-G

19884584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53708644-C-T

http://identifiers.org/hco/3/GRCh38#19884620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53708680-A-C

19884639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708705-A-T

19884647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708713-A-G

19884673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708739-C-T

http://identifiers.org/hco/3/GRCh38#19884676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53708742-C-A

19884676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708742-C-G

19884676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708742-C-T

http://identifiers.org/hco/3/GRCh38#19884707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53708997-C-A

19884707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53708997-C-T

http://identifiers.org/hco/3/GRCh38#19884716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53709006-C-A

19884716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709006-C-T

http://identifiers.org/hco/3/GRCh38#19884718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53709008-A-C

19884735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709026-T-C

19884736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709027-G-T

http://identifiers.org/hco/3/GRCh38#19884740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53709033-C-A

19884835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709123-C-T

19885251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709298-T-C

19885347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709862-G-A

19885347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709862-G-C

19885347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53709862-G-T

19885522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53710096-T-C

19885556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53710134-G-A

19885556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53710134-G-T

19885566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53710144-A-G

http://identifiers.org/hco/3/GRCh38#19886400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53712393-A-C

19886816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53712523-C-T

19886877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53712597-T-G

19888453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53720500-T-C

19888453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53720500-T-G

http://identifiers.org/hco/3/GRCh38#19888466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#53720513-A-C

19888466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53720513-A-G

19888466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 53720513-A-T

19888526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53720573-A-G

http://identifiers.org/hco/3/GRCh38#19888758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53720779-C-A

http://identifiers.org/hco/3/GRCh38#19888776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53720793-C-A

19894180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53722627-C-T

19894183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53722630-C-T

19894382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53722977-T-C

19894383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53722978-A-G

19894520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53723116-G-T

19896126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53728631-T-C

http://identifiers.org/hco/3/GRCh38#19896152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53728657-C-A

19896197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53728700-A-T

http://identifiers.org/hco/3/GRCh38#19896505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53728719-C-A

19896505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53728719-C-T

19896512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53728726-A-G

19896578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53728792-G-A

19896578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53728792-G-T

19896579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53728793-T-C

http://identifiers.org/hco/3/GRCh38#19896621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53728838-A-C

19896621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53728838-A-T

19896654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53728867-T-C

http://identifiers.org/hco/3/GRCh38#19896656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53728869-C-A

19896656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53728869-C-T

19896796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53729012-C-T

19896856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53729072-A-G

19896884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53729100-T-C

19896900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53729109-T-C

19896921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53729138-T-A

http://identifiers.org/hco/3/GRCh38#19896926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53729143-C-A

19896936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53729153-G-A

19896936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53729153-G-T

19898266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53731392-T-C

19898432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53732618-G-C

19898510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53732681-T-C

19898571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53732727-G-A

http://identifiers.org/hco/3/GRCh38#19898628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53732777-A-C

19898628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53732777-A-G

19898663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53732802-G-A

19898663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53732802-G-T

19898929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53733382-G-A

19899169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53733562-G-T

19899217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53733607-T-C

19899372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53733862-A-G

19899397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53733898-A-G

http://identifiers.org/hco/3/GRCh38#19899604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53734108-C-A

19899604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53734108-C-T

19899665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53734159-T-C

19899665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53734159-T-G

19905440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53743931-A-G

19905454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53743945-G-A

http://identifiers.org/hco/3/GRCh38#19905505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53743994-C-A

19905505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53743994-C-T

19905597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53744089-G-A

http://identifiers.org/hco/3/GRCh38#19905674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53744166-A-C

19905707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53744199-C-G

19905721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53744213-T-C

19906021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53744634-G-C

19906340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53745002-G-A

19906561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53745248-C-T

http://identifiers.org/hco/3/GRCh38#19906605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53745275-A-C

19906797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53745372-C-T

19906924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53745500-T-G

http://identifiers.org/hco/3/GRCh38#19908098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53749044-A-C

http://identifiers.org/hco/3/GRCh38#19908148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53749093-C-A

http://identifiers.org/hco/3/GRCh38#19908201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53749136-A-C

19908330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53749246-C-T

19908338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53749254-G-A

19914377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53751094-C-T

19914378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53751095-T-C

19914401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53751118-G-A

19914465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53751169-G-A

19915181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53752638-T-C

19915192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53752663-T-C

19915279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53752749-C-T

19915439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53752909-T-A

http://identifiers.org/hco/3/GRCh38#19915447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53752916-C-A

19915447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53752916-C-T

19915651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53753062-G-C

19915712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53753079-G-A

19915783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53753126-G-A

19916213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53753515-G-C

http://identifiers.org/hco/3/GRCh38#19918134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53756326-C-A

19918134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756326-C-T

19918143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756335-A-G

http://identifiers.org/hco/3/GRCh38#19918152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53756344-C-A

http://identifiers.org/hco/3/GRCh38#19918211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53756398-C-A

19918211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756398-C-G

19918211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756398-C-T

19918302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53756483-G-A

19918317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53756498-T-C

http://identifiers.org/hco/3/GRCh38#19918452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53756628-A-C

19918452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756628-A-G

19918452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756628-A-T

http://identifiers.org/hco/3/GRCh38#19918507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53756670-C-A

19918507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53756670-C-T

19919535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53758302-A-G

19919549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53758316-C-T

19919642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53758402-T-C

19919791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53758532-G-T

19919857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53758603-T-G

19920367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759458-G-T

19920380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759471-G-A

19920380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759471-G-T

19920396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759487-G-A

19920396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759487-G-T

http://identifiers.org/hco/3/GRCh38#19920398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53759489-C-A

19920398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759489-C-T

http://identifiers.org/hco/3/GRCh38#19920401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53759492-C-A

19920401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759492-C-T

19920424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759516-A-G

19920473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759566-T-C

19920473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759566-T-G

19920479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759572-T-C

19920497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53759581-G-A

19920508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53759592-G-A

19920508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53759592-G-T

http://identifiers.org/hco/3/GRCh38#19920549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53759633-C-A

19920585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759668-G-A

19920585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759668-G-T

19920587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759670-G-A

19920602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759684-G-T

19920606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759687-G-T

http://identifiers.org/hco/3/GRCh38#19920615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53759696-C-A

19920661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759742-G-A

19920661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759742-G-T

19920671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759750-T-C

http://identifiers.org/hco/3/GRCh38#19920674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53759753-C-A

19920698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759780-G-A

19920698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53759780-G-T

19932908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53768509-T-C

19933054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53768662-G-C

19933159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769365-T-A

19933166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769372-A-G

19933167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769373-T-A

19933176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769382-T-G

19933180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769386-G-A

19933180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769386-G-C

19933180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53769386-G-T

19933295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53769524-G-A

19933295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53769524-G-T

19933319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53769548-C-T

19933563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53769792-T-C

19933575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53769804-A-G

http://identifiers.org/hco/3/GRCh38#19933628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53769857-C-A

19933628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53769857-C-G

19933628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53769857-C-T

19933655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53769884-G-A

19933671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53769900-A-G

http://identifiers.org/hco/3/GRCh38#19933782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53770014-A-C

http://identifiers.org/hco/3/GRCh38#19934055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53770240-C-A

19934055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53770240-C-T

19934129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53770299-A-G

19934269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770417-C-G

19934351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770491-T-A

19934361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770501-T-C

19934361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770501-T-G

http://identifiers.org/hco/3/GRCh38#19934385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53770524-C-A

19934413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770541-T-C

19934419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770547-T-C

19934431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53770559-T-A

19934747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53771015-G-T

19934763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53771031-G-A

19945297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53777444-G-A

19945297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53777444-G-C

19945595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53778794-G-T

19945619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53778819-C-T

19945767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53778963-T-G

http://identifiers.org/hco/3/GRCh38#19945837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53779031-C-A

19945837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron variant
orthologous variants: 53779031-C-T

http://identifiers.org/hco/3/GRCh38#19946186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#53785313-C-A

19946214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53785330-T-A

19946575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53785635-C-T

19946688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53785715-C-G

19946749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53785800-C-T

19946984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26330
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53786067-A-G