http://identifiers.org/hco/5/GRCh38#154329378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57627607-A-C

154329378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627607-A-T

154329379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627608-T-A

154329379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627608-T-C

154329379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627608-T-G

http://identifiers.org/hco/5/GRCh38#154329458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57627680-C-A

154329458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627680-C-T

154329482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627704-G-A

154329482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627704-G-T

http://identifiers.org/hco/5/GRCh38#154329489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57627711-A-C

154329489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627711-A-G

http://identifiers.org/hco/5/GRCh38#154329500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57627722-C-A

154329500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627722-C-T

http://identifiers.org/hco/5/GRCh38#154329515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57627737-C-A

154329515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627737-C-G

154329518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627740-T-G

154329519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627741-T-A

http://identifiers.org/hco/5/GRCh38#154329719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57627951-C-A

154329719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57627951-C-T

154329771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628001-T-A

154329771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628001-T-C

154329787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628011-A-G

http://identifiers.org/hco/5/GRCh38#154329790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57628014-C-A

154329790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628014-C-T

http://identifiers.org/hco/5/GRCh38#154329826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57628078-C-A

154329826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628078-C-T

154329920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628154-A-G

154329920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628154-A-T

154329960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 57628194-G-A

154329960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 57628194-G-C

154329960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 57628194-G-T

154329980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628204-G-A

154329980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628204-G-C

154329980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628204-G-T

154329993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628217-A-T

http://identifiers.org/hco/5/GRCh38#154329999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57628223-A-C

http://identifiers.org/hco/5/GRCh38#154330002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57628226-C-A

154330002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628226-C-G

154330015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628247-G-C

154330015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57628247-G-T

154330641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57629039-T-G

http://identifiers.org/hco/5/GRCh38#154334595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57629849-A-C

154339386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57630321-T-C

http://identifiers.org/hco/5/GRCh38#154339520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57630456-C-A

154339631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57630564-T-C

154339704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57630630-G-A

154342622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57633291-A-G

154343038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57633724-G-A

154343550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57635154-G-A

154343788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57635385-A-T

154344680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57635535-A-T

154344735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57635589-G-T

154344756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57635610-A-G

154353237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637059-G-A

154353298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637118-G-A

154353298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637118-G-C

154353298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637118-G-T

http://identifiers.org/hco/5/GRCh38#154353299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57637119-C-A

154353299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637119-C-G

154353423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637197-G-T

154353505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637266-G-A

154353725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57637457-G-A

154358977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57638629-C-T

154359057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57638708-T-A

154359127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57638778-G-A

154359214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57638861-G-A

154359349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57638937-G-T

http://identifiers.org/hco/5/GRCh38#154359521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57639082-C-A

154359521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57639082-C-T

154360853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57640485-G-A

154360866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57640489-G-T

154360947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57640571-T-C

154361099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57640724-G-T

154361782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641288-C-T

154361930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641419-G-A

154362003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641467-G-A

154362189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641653-G-A

154362189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641653-G-C

154362240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641700-C-T

http://identifiers.org/hco/5/GRCh38#154362329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57641788-C-A

154362377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641843-G-A

154362392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57641857-T-A

154362690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57642138-T-C

154362923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57642288-G-A

154363004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57642347-C-T

154363200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57642542-A-G

154363557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643001-G-T

154363717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643161-A-G

154363723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643167-G-A

154363747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643191-G-A

154364116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643539-G-T

154364198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643618-G-A

154364300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643720-A-G

154364302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643722-A-G

154364367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57643746-T-C

154364561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57644337-G-A

154364641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57644418-T-C

154364761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57644536-A-G

154364807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57644581-A-G

154365106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57644829-T-C

154365279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57644998-T-C

http://identifiers.org/hco/5/GRCh38#154365504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57645162-A-C

154366201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57647121-T-C

154366216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57647136-T-G

154366255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57647177-A-T

154366627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57647458-T-C

154369438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57648947-G-A

154370157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57649542-T-G

154370269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57649661-G-A

154373556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57651293-A-T

154374068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57651798-C-T

154374088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57651806-A-G

154374110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57651827-T-C

154375465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57655608-G-C

154375810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57655967-G-A

154376003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656164-A-G

http://identifiers.org/hco/5/GRCh38#154376220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57656336-C-A

154376238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656345-G-A

154376335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656444-T-G

154376389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656498-G-A

154376405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656514-A-G

154376502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656594-A-G

http://identifiers.org/hco/5/GRCh38#154376544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57656626-C-A

154376580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656657-G-A

154376580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57656657-G-T

154376912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57657148-C-G

154376969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57657218-A-T

154377126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57657337-C-G

154377175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57657393-G-A

http://identifiers.org/hco/5/GRCh38#154377346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57657541-C-A

154377700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57657790-C-T

154377915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57657993-C-T

154378110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57658128-A-G

154378219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57658199-A-G

154378894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57658840-A-G

154379045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57658989-C-T

154379103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659043-T-A

154379358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659440-C-T

154379493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659557-C-T

154379545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659609-C-T

http://identifiers.org/hco/5/GRCh38#154379632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57659687-C-A

154379687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659724-A-G

http://identifiers.org/hco/5/GRCh38#154379737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57659775-C-A

154379844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659853-G-A

154379986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659975-G-A

154380020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659983-G-A

154380020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57659983-G-T

154380228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660175-T-C

154380330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660235-G-T

http://identifiers.org/hco/5/GRCh38#154380349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57660242-C-A

154380349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660242-C-T

http://identifiers.org/hco/5/GRCh38#154380350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57660243-A-C

154380388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660269-G-A

154380388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660269-G-C

154380388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660269-G-T

154380391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660271-G-A

154380466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660336-G-A

154380542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660412-C-G

154380542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660412-C-T

154380599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660469-A-G

http://identifiers.org/hco/5/GRCh38#154380652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57660522-C-A

154380652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660522-C-T

http://identifiers.org/hco/5/GRCh38#154380678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57660546-A-C

154380678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660546-A-G

154380678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660546-A-T

154380704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660565-T-C

http://identifiers.org/hco/5/GRCh38#154380714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57660575-C-A

154380721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660580-A-G

http://identifiers.org/hco/5/GRCh38#154380733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57660592-A-C

154380733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660592-A-G

154380733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660592-A-T

154384512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660698-C-T

154384758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660875-G-A

154384758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57660875-G-C

http://identifiers.org/hco/5/GRCh38#154385320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57661328-A-C

154386184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662206-G-T

http://identifiers.org/hco/5/GRCh38#154386189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57662211-C-A

http://identifiers.org/hco/5/GRCh38#154386197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57662217-C-A

154386197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662217-C-G

154386197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662217-C-T

154386205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662225-A-G

154386205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662225-A-T

154386228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662237-G-A

154386228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662237-G-T

154386293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662276-A-G

154386373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662354-C-G

154386373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662354-C-T

154386510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662442-G-A

154386510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662442-G-C

154386512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662444-G-C

154386512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662444-G-T

http://identifiers.org/hco/5/GRCh38#154386587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57662486-C-A

154386607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662500-G-A

154386607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662500-G-T

154386612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662505-T-A

154386612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662505-T-G

154386652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662538-G-T

154386687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662562-T-G

154386688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662563-G-T

154386730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662581-T-C

154386795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662636-C-T

154386801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662642-A-G

154386801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662642-A-T

154386815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662653-G-T

154386839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662702-T-G

http://identifiers.org/hco/5/GRCh38#154386851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57662715-C-A

154386874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662737-A-G

154386912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662775-G-A

154386912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662775-G-T

154386982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662848-A-G

154387094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57662991-A-G

154387116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663013-G-A

154387140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663037-G-T

http://identifiers.org/hco/5/GRCh38#154387153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57663050-C-A

154387354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663238-C-T

154387367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663251-G-T

154387384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663289-C-T

154387435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663379-T-C

http://identifiers.org/hco/5/GRCh38#154387496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57663531-C-A

154387496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663531-C-T

154387513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663548-G-A

154387513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663548-G-T

http://identifiers.org/hco/5/GRCh38#154387529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57663564-C-A

154387539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663574-G-T

154387562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663603-T-C

154387736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663737-A-G

154387777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663783-T-A

154387777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57663783-T-G

154390692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57664618-A-G

154390914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57664852-G-T

154391010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57664945-C-T

154391054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57665000-G-T

154391255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57665134-T-C

154391271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57665156-G-A

154400551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57666763-G-A

154401409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667552-C-G

154401409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667552-C-T

154401410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667553-G-A

154401468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667604-A-G

154401469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667605-G-A

154401530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667702-T-G

154401617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57667789-T-C

154401944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668051-G-A

154402024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668112-T-C

154402195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668220-C-T

154402211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668236-G-A

154403937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668325-G-A

154403937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668325-G-T

http://identifiers.org/hco/5/GRCh38#154404338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57668657-C-A

154404338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668657-C-T

154404350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668669-G-T

154404402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57668706-C-G

http://identifiers.org/hco/5/GRCh38#154404419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57668722-A-C

154404913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57669054-G-C

154404953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57669100-T-A

154407631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57670382-A-G

154407761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57670496-C-T

154407841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57670535-G-C

http://identifiers.org/hco/5/GRCh38#154408154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57670805-C-A

154408215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57670850-A-G

154408300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57670943-C-G

http://identifiers.org/hco/5/GRCh38#154408303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57670946-A-C

154409603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57671938-G-A

154409603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57671938-G-C

154409744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672079-G-A

154409750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672085-A-T

154409770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 57672105-T-C

154409784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672119-G-A

154412411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672659-C-T

154412433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672681-T-C

154412506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672752-T-C

154412597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672844-C-T

154412724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672882-G-T

154412793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672944-A-G

154412793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672944-A-T

154412796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672947-G-A

154412796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672947-G-T

http://identifiers.org/hco/5/GRCh38#154412804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57672955-C-A

154412804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672955-C-T

154412823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672973-T-C

154412824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672974-G-C

154412839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57672988-G-T

154415914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674647-G-A

154415914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674647-G-T

154415917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674650-G-A

154415949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674689-G-C

154415952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674692-G-A

154415960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674702-C-T

154415970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674720-A-G

154415970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674720-A-T

154416030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674781-T-C

http://identifiers.org/hco/5/GRCh38#154416042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57674793-C-A

http://identifiers.org/hco/5/GRCh38#154416046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57674797-C-A

154416076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674810-G-T

154416084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674818-A-G

154416268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674948-C-T

154416328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57674979-G-A

154416458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675033-T-A

154416458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675033-T-G

154416528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675083-C-T

154416668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675276-T-G

154416669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675277-G-C

154416669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675277-G-T

154416679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675287-G-A

154416679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675287-G-T

http://identifiers.org/hco/5/GRCh38#154416689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57675309-A-C

154416705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675326-G-T

154416708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675329-A-T

http://identifiers.org/hco/5/GRCh38#154416777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57675359-C-A

154416777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675359-C-T

154416873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675455-T-C

154417148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675665-G-A

154417148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675665-G-T

154417161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675678-G-A

154417161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675678-G-T

154417292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675782-A-G

154417393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675853-G-A

154417393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675853-G-T

154417422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675867-G-A

154417422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675867-G-T

http://identifiers.org/hco/5/GRCh38#154417434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57675880-C-A

154417434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675880-C-T

154417510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675934-G-A

154417510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675934-G-T

154417535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675942-G-A

154417535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675942-G-C

154417535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675942-G-T

154417553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675960-A-G

154417556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57675963-G-A

154417611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676014-G-T

http://identifiers.org/hco/5/GRCh38#154417650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676032-C-A

154417650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676032-C-T

154417747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676117-T-C

154417787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676135-G-A

154417787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676135-G-T

http://identifiers.org/hco/5/GRCh38#154417835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676171-C-A

http://identifiers.org/hco/5/GRCh38#154417868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676208-C-A

154418020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676336-T-C

154418105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676389-G-A

154418173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676432-G-A

154418173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676432-G-T

154418225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676451-T-C

http://identifiers.org/hco/5/GRCh38#154418229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676455-A-C

154418467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676527-G-T

154418480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676540-C-T

http://identifiers.org/hco/5/GRCh38#154418575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676566-A-C

154418575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676566-A-G

154418603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676594-G-T

http://identifiers.org/hco/5/GRCh38#154418697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676639-C-A

154418699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676641-G-T

154418720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676662-T-C

154418967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676854-C-T

154418982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676869-T-C

154419085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676977-G-T

154419108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676990-G-A

http://identifiers.org/hco/5/GRCh38#154419109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57676991-C-A

154419109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676991-C-T

154419112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57676994-T-C

154419124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677006-G-A

154419124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677006-G-T

154419141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677021-T-C

154419183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677056-T-C

154419207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677081-T-C

http://identifiers.org/hco/5/GRCh38#154419235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677100-C-A

154419235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677100-C-T

http://identifiers.org/hco/5/GRCh38#154419240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677105-C-A

154419240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677105-C-T

154419414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677178-G-A

http://identifiers.org/hco/5/GRCh38#154419452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677208-C-A

154419508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677244-A-G

http://identifiers.org/hco/5/GRCh38#154419525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677261-C-A

154419543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677284-G-T

http://identifiers.org/hco/5/GRCh38#154419566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677309-C-A

http://identifiers.org/hco/5/GRCh38#154419600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677343-C-A

154419600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677343-C-T

154419635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677377-T-C

http://identifiers.org/hco/5/GRCh38#154419652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677394-C-A

154419658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677400-A-G

154419746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677464-T-C

154419806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677515-T-C

154419867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677550-G-T

154419952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677620-G-T

http://identifiers.org/hco/5/GRCh38#154419961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57677629-C-A

154419961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677629-C-T

154419966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677634-G-A

154419966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677634-G-T

154420126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677755-A-G

154420302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677839-A-G

154420423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57677899-A-G

154420728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57678132-C-T

154420815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57678162-G-C

http://identifiers.org/hco/5/GRCh38#154420862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#57678207-C-A

154420862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57678207-C-T

http://identifiers.org/hco/5/GRCh38#154421027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57678367-C-A

154421098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678443-A-G

154421106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678449-A-G

154421120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678463-A-G

154421179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678516-G-C

154421307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678620-G-C

154421758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678727-C-T

154421980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57678884-C-T

http://identifiers.org/hco/5/GRCh38#154438870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57683487-C-A

154438870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683487-C-G

154438870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57683487-C-T

http://identifiers.org/hco/5/GRCh38#154444307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57689817-C-A

154444307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57689817-C-T

http://identifiers.org/hco/5/GRCh38#154445742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57692191-C-A

154445742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: 57692191-C-T

154445752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: 57692201-G-A

154445752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: 57692201-G-C

154445752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: 57692201-G-T

154445761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: 57692213-T-C

http://identifiers.org/hco/5/GRCh38#154445786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26760
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#57692237-C-A