http://identifiers.org/hco/11/GRCh38#126543852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34835624-C-A

126543852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835624-C-T

126543894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835582-G-T

126544012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835463-G-A

126544012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835463-G-T

126544024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835439-C-T

126544041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835423-G-A

http://identifiers.org/hco/11/GRCh38#126544145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34835319-A-C

126544145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34835319-A-G

http://identifiers.org/hco/11/GRCh38#126544243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34835221-C-A

126544243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 34835221-C-T

126545710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833911-G-T

126545739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833882-G-A

126545856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833790-C-T

126545887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833753-G-A

126545887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833753-G-C

http://identifiers.org/hco/11/GRCh38#126545967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34833670-A-C

126545982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833642-C-T

126546002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833616-G-A

126546012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833606-T-G

126546071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833553-A-G

126546077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833547-T-C

126546138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833486-C-T

126546423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833217-A-G

126546563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833109-G-A

126546637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34833035-G-C

126546986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832809-T-C

126547061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832744-T-A

126548319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832398-C-G

126548319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832398-C-T

126548358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832358-T-C

126548358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832358-T-G

126548452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832247-C-G

126548452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832247-C-T

126548534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34832167-C-T

http://identifiers.org/hco/11/GRCh38#126548603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34832100-C-A

http://identifiers.org/hco/11/GRCh38#126548962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34831761-C-A

http://identifiers.org/hco/11/GRCh38#126549435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34831292-C-A

126549500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34831225-T-C

126549698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830960-C-T

126549710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830950-C-T

126549712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830948-T-A

126549813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830848-G-A

126549813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830848-G-T

126549886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830707-T-C

126550020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830575-T-C

126550047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830548-C-T

126550200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830406-G-A

126550245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34830360-A-G

126556968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34827306-G-C

http://identifiers.org/hco/11/GRCh38#126557047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34827225-A-C

126557059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34827213-A-G

126557290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826994-A-G

126557292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826992-G-A

126557295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34826989-T-C

126560203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825793-C-T

126560284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825714-C-T

126560568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825421-T-C

126560568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825421-T-G

126560921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825060-T-C

126560921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34825060-T-G

126561048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824933-C-T

126561112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824826-G-A

126561227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824741-T-G

126561344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824621-A-T

126561399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34824566-T-C

126561529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34824437-C-T

126561555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34824411-T-C

126561732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824225-T-A

126561853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34824103-G-T

126562143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823825-A-G

126562370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823594-G-A

126562591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823403-C-T

126562598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823388-G-A

http://identifiers.org/hco/11/GRCh38#126562694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34823304-C-A

126562817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823173-G-A

126562973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823028-G-A

126562973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823028-G-C

126562973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823028-G-T

126562995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823003-G-A

126562995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34823003-G-T

126563017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822995-G-A

126563017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822995-G-T

http://identifiers.org/hco/11/GRCh38#126563208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34822817-C-A

126563208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822817-C-T

126563229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822803-C-T

126563476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822569-T-C

http://identifiers.org/hco/11/GRCh38#126563573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34822472-A-C

126563869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822181-C-G

126563967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34822095-C-T

126564126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34821926-C-T

126564326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34821527-A-G

126564326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34821527-A-T

http://identifiers.org/hco/11/GRCh38#126564557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34821321-C-A

http://identifiers.org/hco/11/GRCh38#126564581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34821291-C-A

126564585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34821287-C-T

http://identifiers.org/hco/11/GRCh38#126564674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#34821199-C-A

http://identifiers.org/hco/11/GRCh38#126564901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34820979-C-A

126564901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820979-C-T

126565005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820876-G-A

126565371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820532-T-G

126565399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820504-G-C

126565556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820344-G-A

126565877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34820025-G-A

126566012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819921-A-G

126566394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819579-T-C

126566419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819553-T-C

126566424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819548-G-A

126566470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819501-G-T

126566481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819490-A-G

126566533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819434-G-T

126566661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819294-A-G

126566661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819294-A-T

126566690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819265-C-T

126566694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819261-T-A

126566731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819227-A-G

126566764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819193-G-A

126566764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819193-G-T

126566796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819153-T-A

126566901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819052-A-T

126566924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34819023-C-T

126567092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818866-T-G

126567578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818146-C-G

126567679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34818024-G-C

126567819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817920-G-T

http://identifiers.org/hco/11/GRCh38#126567865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34817887-C-A

126567865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817887-C-T

126567943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817809-A-T

http://identifiers.org/hco/11/GRCh38#126568086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34817083-C-A

126568086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34817083-C-T

126568204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816984-A-G

126568361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816840-G-A

126568456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816731-C-T

http://identifiers.org/hco/11/GRCh38#126568650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34816549-C-A

126568659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816540-C-G

126568877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816331-G-A

126568886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816322-C-T

126568892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816316-G-A

126568908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816300-A-G

http://identifiers.org/hco/11/GRCh38#126569069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34816175-A-C

126569128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34816110-C-G

126569731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815172-G-A

126569737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815166-G-A

126569765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815138-T-G

126569811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815095-G-A

126569903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34815005-T-C

126569950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814955-C-G

http://identifiers.org/hco/11/GRCh38#126570009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34814896-A-C

126570473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814428-G-C

126570668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814246-A-G

126570698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814217-C-G

126570698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814217-C-T

126570734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814179-T-C

http://identifiers.org/hco/11/GRCh38#126570736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34814177-A-C

126570799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34814112-G-A

126570976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813697-T-G

126571270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813338-A-G

126571624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34813030-T-C

126571917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812766-G-A

126571917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812766-G-C

126572047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812623-G-T

126572053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812617-T-A

126572111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812558-C-T

126572184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812487-G-T

126573229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812430-G-C

http://identifiers.org/hco/11/GRCh38#126573479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34812139-A-C

126573479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812139-A-G

http://identifiers.org/hco/11/GRCh38#126573486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34812132-A-C

126573486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34812132-A-T

http://identifiers.org/hco/11/GRCh38#126573733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34811886-A-C

126573733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811886-A-G

126573785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811819-A-G

http://identifiers.org/hco/11/GRCh38#126573948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34811700-C-A

126574172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811471-T-G

126574173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811470-C-T

126574203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811440-G-A

126574220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811421-C-T

126574504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34811151-T-G

126574691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810947-G-A

126574830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34810810-G-A

126576160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806063-G-A

126576178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34806045-G-A

126576583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805814-A-G

http://identifiers.org/hco/11/GRCh38#126576631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34805770-A-C

126576789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805636-G-A

126576876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805556-C-T

126576926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805508-T-G

126577382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805044-A-T

126577419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34805014-G-A

126577890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804866-T-A

126577890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804866-T-C

126578067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804713-T-C

126578244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804650-T-C

126578265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804629-T-C

126578528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804419-G-A

126578528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804419-G-T

126578536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804410-G-A

126578536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804410-G-C

126578562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804373-G-A

126578590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804346-G-A

126578659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804295-C-T

126578868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34804098-T-C

126579032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803928-G-A

126579032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803928-G-C

126579226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803719-C-T

126579505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803438-C-T

http://identifiers.org/hco/11/GRCh38#126579554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34803390-A-C

126579743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803236-C-T

126579978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803128-T-C

126580222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34803073-G-C

126580444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802839-G-A

126580444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802839-G-C

126580601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802705-C-T

126580739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802580-C-G

126580832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802506-T-C

126580862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802480-C-T

126580949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34802412-G-C

126582215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801193-A-T

126582296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34801112-C-T

126583437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34800105-C-T

126583558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799971-G-A

126584049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799528-A-G

126584051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799526-C-T

126584188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799382-C-T

126584495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799114-G-C

126584605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799052-T-G

126584622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34799035-A-T

126584712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798927-G-A

126584712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798927-G-T

126585508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798782-A-G

126585585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798714-C-T

126585763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798539-G-A

126585782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798520-G-T

126585783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798519-G-T

126585959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798345-G-A

126586103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798202-C-T

126586295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798044-G-A

126586295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34798044-G-T

126586534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34797790-G-A

126586581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796629-G-A

126586592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796618-C-T

126586696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796517-C-T

126586716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34796496-G-A

126587482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34795130-C-T

http://identifiers.org/hco/11/GRCh38#126587587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34795029-A-C

http://identifiers.org/hco/11/GRCh38#126587646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34794982-C-A

126587646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794982-C-T

126587901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794721-G-A

126587907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794715-C-T

126588018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794602-T-G

126588108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794512-A-G

126588223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794401-A-T

126588289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794355-A-G

http://identifiers.org/hco/11/GRCh38#126588341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34794310-A-C

126588453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794031-G-A

126588621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793892-A-G

126589105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793473-G-A

126589105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793473-G-C

126589153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793425-C-T

126589175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793403-A-G

126589396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793223-C-T

http://identifiers.org/hco/11/GRCh38#126589449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34793171-A-C

126589473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793138-A-G

126589596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792949-A-T

126589605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792907-C-G

126589614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792885-A-G

http://identifiers.org/hco/11/GRCh38#126589726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34792586-C-A

126589893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792416-G-A

126589918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792389-T-A

126590177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792170-T-C

126590190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792154-C-T

126590249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792095-T-A

126590255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792089-G-C

126590287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791584-T-A

126590581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791344-A-G

126590683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791218-G-A

126590715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791186-G-C

126590783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791124-T-A

126590783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791124-T-C

126591407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790836-G-A

126591476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790766-C-T

126591576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790628-C-G

126591866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789393-G-A

126591970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789309-C-G

126591970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789309-C-T

126591994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789285-G-A

126592111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789167-T-G

126592441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789015-G-A

126592529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788955-G-A

126592529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788955-G-T

126592651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788823-A-G

126592747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788707-G-A

126592886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788595-A-T

126592924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788577-G-A

126592938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788563-T-C

126593003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788532-G-A

126593137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788397-G-T

126593177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788360-T-C

126593261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788287-G-A

126593475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788049-G-A

126593747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787794-T-C

126593810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787733-C-G

126593887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787661-C-T

126593959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787589-C-G

126593959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787589-C-T

126594043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787488-A-G

126594771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787070-G-A

126594771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787070-G-C

126594876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786976-C-G

126594992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786858-G-A

http://identifiers.org/hco/11/GRCh38#126595312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34786597-A-C

126595439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786545-T-C

126595594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786455-G-A

http://identifiers.org/hco/11/GRCh38#126595683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34786386-C-A

126595683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786386-C-T

126595979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786199-C-T

126595984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786194-G-A

126596101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786101-A-G

126596188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786032-G-A

126596388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34785839-T-G

http://identifiers.org/hco/11/GRCh38#126596415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34785814-C-A

126596425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34785804-C-G

126596615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34785642-C-T

126596720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34785554-A-G

126597249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34784691-G-A

126597249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34784691-G-C

126597803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34784221-G-A

126597803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34784221-G-T

126597868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34784172-T-C

126597887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34784153-A-G

126598061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783982-C-G

126598111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783951-C-T

126598368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783753-T-C

126598525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783566-C-T

126598534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783557-T-C

126598818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783283-G-A

126598819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783282-G-A

126599033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783091-T-C

126599119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34783001-C-T

126599608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34782531-C-T

126599675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34782507-C-T

126601070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34780227-T-C

126601733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779543-G-A

126601747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779531-A-G

126601953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34779318-C-T

http://identifiers.org/hco/11/GRCh38#126601973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#34779298-C-A

126602213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779115-C-G

126602311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34779054-A-G

http://identifiers.org/hco/11/GRCh38#126602393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34778998-C-A

126602601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778808-G-A

126602631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778773-C-T

126602682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778733-G-A

126602993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34778454-A-G

126603588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777214-A-G

126603663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34777144-G-C

126603839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776966-G-A

126603839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776966-G-C

126604051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776802-T-C

126604053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776800-C-T

126604073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776784-C-G

126604359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776202-T-C

126604461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34776096-C-T

126604892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775803-C-G

126604969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775740-G-A

126605103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775611-G-A

126605427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775268-G-A

126605446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775231-G-A

126605449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775228-G-A

126605541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775136-C-T

126605664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34775014-A-G

126605791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774911-G-A

126605987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774711-G-T

126606006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774685-A-G

126606031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774660-C-T

126606256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774452-T-C

126606298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774407-G-A

126606298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774407-G-C

126606430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774289-A-G

126606432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774287-G-A

126606525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774171-G-T

126606620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774086-C-T

126606650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34774026-T-A

126606814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773872-A-G

126606833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773837-A-G

126606978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773741-G-T

126607027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773698-G-T

126607034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773691-C-T

126607035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773690-T-G

126607076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34773639-G-A

126607377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34773361-G-A

126607682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34773071-A-G

126607879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772874-A-G

126607937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34772825-G-C

126608275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772561-C-T

126608277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772559-T-G

126608287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772521-C-G

126608287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772521-C-T

126608381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772424-C-G

126608381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772424-C-T

126608801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34772062-G-A

126608907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34771945-G-A

http://identifiers.org/hco/11/GRCh38#126609014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34771848-A-C

126609133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34771748-G-A

126609156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34771732-G-A

126609440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34771470-G-A

126609489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34771428-A-G

126609852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770592-A-T

126609933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770513-G-A

126609963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770484-A-G

126610190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770328-A-G

http://identifiers.org/hco/11/GRCh38#126610249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34770308-C-A

126610249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770308-C-T

126610551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770145-G-T

126610586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770109-G-A

126610630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34770066-A-G

126610657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34770039-G-A

126610658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34770038-C-G

126610658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34770038-C-T

126610675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34770021-G-T

126610678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34770018-A-G

126610700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34769996-T-C

126610701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34769995-G-A

126610903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34769846-T-G

126610990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34769775-A-T

http://identifiers.org/hco/11/GRCh38#126611000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#34769765-C-A

126611012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34769753-A-T