117476164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395983-G-A

117476374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396205-A-G

117486359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396304-T-C

117486381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396326-G-A

117486382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396327-T-G

http://identifiers.org/hco/10/GRCh38#117486449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59396394-C-A

117486534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396462-T-C

117486618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396529-A-G

117486626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396537-T-A

117486626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396537-T-C

117486626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396537-T-G

http://identifiers.org/hco/10/GRCh38#117486797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59396705-A-C

117486797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396705-A-G

117486991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59396891-C-T

http://identifiers.org/hco/10/GRCh38#117489365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398512-C-A

117489365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398512-C-T

117489374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398522-G-A

117489374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398522-G-T

http://identifiers.org/hco/10/GRCh38#117489375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398523-C-A

http://identifiers.org/hco/10/GRCh38#117489379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398527-C-A

117489379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398527-C-G

117489421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398567-A-G

http://identifiers.org/hco/10/GRCh38#117489426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398572-C-A

http://identifiers.org/hco/10/GRCh38#117489477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398597-C-A

117489497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398617-T-C

117489529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398647-G-A

117489529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398647-G-T

117489575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398688-G-T

117489582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398695-A-G

117489592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398708-G-T

117489593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398709-A-G

http://identifiers.org/hco/10/GRCh38#117489631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398746-C-A

117489642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398755-G-A

117489642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398755-G-T

117489770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398856-G-T

http://identifiers.org/hco/10/GRCh38#117489788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59398866-C-A

117489838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398902-G-T

117489853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398917-G-T

117489933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398997-G-A

117489933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59398997-G-T

117490102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399145-T-A

http://identifiers.org/hco/10/GRCh38#117490126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59399160-A-C

117490139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399169-T-C

117490230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399259-T-A

117490230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399259-T-C

117490268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399295-G-A

117490290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399320-C-T

117490326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399356-A-G

117490387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399391-G-A

117490387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399391-G-T

117490522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399504-T-C

117490612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399590-A-G

http://identifiers.org/hco/10/GRCh38#117490614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59399592-C-A

117490614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399592-C-T

117490753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399742-G-T

117490871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59399811-C-T

http://identifiers.org/hco/10/GRCh38#117490954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59399889-C-A

117491254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400174-A-G

117491262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400182-A-T

117491411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400315-C-T

117491461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400365-T-C

117491482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400386-C-T

117496358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406345-G-A

117496792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406722-G-A

117496793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406723-G-C

117496853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59406795-T-C

http://identifiers.org/hco/10/GRCh38#117497501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59407129-C-A

117497501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407129-C-T

117497551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407179-G-A

117497657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407292-T-C

117497777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407455-A-G

117497974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407792-G-A

117498017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407834-G-A

117498128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407955-G-C

117499246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59408611-A-G

117499265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59408632-G-A

117499476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59408805-A-T

117499477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59408806-C-T

117499704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59408999-G-A

117499705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409000-T-G

117499706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409001-G-C

117499721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409016-T-C

117499917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409270-C-T

117499934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409287-T-C

http://identifiers.org/hco/10/GRCh38#117500353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59409690-C-A

117500353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409690-C-T

117500445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409768-G-A

117500445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409768-G-C

117500445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409768-G-T

117500462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409785-G-A

117500462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59409785-G-T

117500806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410168-A-G

117500882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410276-C-T

117500889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410283-A-G

117500949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410364-T-C

117501024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410432-C-T

117501026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410434-C-T

117501049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59410451-A-G

117501563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411060-A-G

http://identifiers.org/hco/10/GRCh38#117501591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59411085-C-A

117501591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411085-C-T

117502911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411783-G-A

117502911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411783-G-T

117502942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59411814-C-T

117503294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412195-C-G

117503294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412195-C-T

117503760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59412669-C-T

117503803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413016-T-C

117503809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413022-G-C

117504071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413254-C-T

117504182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413437-C-G

117504182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413437-C-T

117504479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59413743-C-T

117504815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59414072-C-T

http://identifiers.org/hco/10/GRCh38#117505084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59414735-C-A

117505084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59414735-C-T

117505259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59414898-G-A

117505280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59414919-C-T

117506410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59415416-A-G

117508551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59417501-C-T

117508554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59417504-C-T

117509194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418203-C-T

117509434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418430-A-G

117509455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418445-A-G

117509559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418521-A-G

117509629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418591-G-A

117509638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418600-G-T

117512367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420485-T-A

117512455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420568-T-C

117512859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420986-G-A

http://identifiers.org/hco/10/GRCh38#117512920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59421029-A-C

117513166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59421226-C-T

117514467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59422355-C-T

117514556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59422443-C-T

117514573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59422460-C-T

http://identifiers.org/hco/10/GRCh38#117514610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59422483-C-A

117514813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59422867-C-G

117517407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424903-A-G

117517436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424930-T-G

117517555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59425108-G-A

117517590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59425143-C-T

http://identifiers.org/hco/10/GRCh38#117519377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59426330-C-A

117519377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426330-C-T

117519528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426463-G-A

117519771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426676-G-T

117520028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426927-G-A

http://identifiers.org/hco/10/GRCh38#117520953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59427729-C-A

117520997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427774-G-T

117521649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428532-G-C

117521683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428572-A-G

117521753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428634-T-A

117521825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428717-C-T

117521826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428718-T-G

117521974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428855-C-G

117522094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428960-A-G

117522128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428994-A-T

117522342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59429180-A-T

117524950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59431527-G-C

117525034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59431612-C-T

117525075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59431654-A-T

117525277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59432001-T-C

117525359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59432144-G-C

http://identifiers.org/hco/10/GRCh38#117525401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59432194-A-C

117525401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59432194-A-G

117525650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59432473-T-C

117526253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433059-T-C

117526825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433625-C-T

117527431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59434574-C-T

117527908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435044-G-A

117528060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435204-T-C

117529251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435749-C-T

117529484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435948-C-T

117530781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436613-G-A

117530860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436651-C-T

117531086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436853-A-G

117531087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436854-G-A

117531520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437253-G-A

117531520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437253-G-T

117531529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437266-G-A

117532076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437713-G-C

117532076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437713-G-T

117532500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438102-C-T

117532620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438185-G-T

117533018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438564-G-A

117533018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438564-G-C

117533119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59438620-C-T

117533550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439072-C-T

117533634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439126-C-T

117533689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439180-T-C

http://identifiers.org/hco/10/GRCh38#117533700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59439202-C-A

http://identifiers.org/hco/10/GRCh38#117533750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59439249-A-C

117534157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439661-G-A

117534232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439726-G-A

117534232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439726-G-T

117534418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439893-C-T

117534427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439902-G-A

117534427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439902-G-C

117534427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439902-G-T

http://identifiers.org/hco/10/GRCh38#117534430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59439905-C-A

117534460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439941-G-A

117534474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439963-G-T

117534713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440199-G-A

117534747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440232-G-A

117534747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440232-G-C

117534835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440307-T-G

117535002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440468-A-G

117535061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440535-G-A

117535376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440732-C-T

117535521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440859-C-G

117535546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440891-G-A

117535652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440934-G-A

117535963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441212-G-T

117535995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441240-A-G

117536158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441383-C-T

117536199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441421-G-A

117536214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441437-T-G

http://identifiers.org/hco/10/GRCh38#117536265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59441466-C-A

117536455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441626-T-C

http://identifiers.org/hco/10/GRCh38#117536502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59441644-C-A

117536502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441644-C-G

117536508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441650-G-A

http://identifiers.org/hco/10/GRCh38#117536850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59441938-C-A

117536850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441938-C-T

117537009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442083-G-A

117537015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442089-G-A

117537032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442123-T-C

117537043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442134-C-G

http://identifiers.org/hco/10/GRCh38#117537092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59442180-C-A

117537625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59442714-T-C

117537730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442797-C-G

117537730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442797-C-T

117537778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442845-G-A

117537844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442911-G-A

117538090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443088-C-T

117538607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443477-G-C

117539154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59443996-C-T

117539174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444020-T-C

117539591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444332-G-A

117539764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444466-G-T

117539868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444566-G-C

http://identifiers.org/hco/10/GRCh38#117539999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59444659-C-A

117540182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444821-A-G

117540364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444979-T-A

117540432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445041-C-T

http://identifiers.org/hco/10/GRCh38#117541022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59445487-C-A

117541022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445487-C-T

117541024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445489-A-G

117541170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445657-T-C

117541332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445812-G-A

117541542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446024-A-T

117541862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446306-G-T

http://identifiers.org/hco/10/GRCh38#117541987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59446436-C-A

117541987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446436-C-T

117541988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446437-A-T

http://identifiers.org/hco/10/GRCh38#117542217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59446662-C-A

117542217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59446662-C-T

http://identifiers.org/hco/10/GRCh38#117542258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59446703-C-A

117542258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59446703-C-T

117542278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59446723-G-A

117542278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59446723-G-C

117542278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59446723-G-T

117542290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59446735-A-G

117542453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59446892-G-A

117542453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59446892-G-T

117542528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59446970-A-G

117542528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59446970-A-T

117542845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447282-G-C

117542845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447282-G-T

117542879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447304-T-A

http://identifiers.org/hco/10/GRCh38#117543101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59447488-C-A

117543101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447488-C-G

117543101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447488-C-T

http://identifiers.org/hco/10/GRCh38#117543106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59447493-C-A

117543106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447493-C-G

117543106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447493-C-T

117543162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447542-G-A

117543162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447542-G-C

117543162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447542-G-T

http://identifiers.org/hco/10/GRCh38#117543166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59447546-C-A

117543166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447546-C-T

http://identifiers.org/hco/10/GRCh38#117543497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59447880-A-C

http://identifiers.org/hco/10/GRCh38#117543506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59447889-A-C

117543506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447889-A-G

http://identifiers.org/hco/10/GRCh38#117543519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#59447902-A-C

117543519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59447902-A-G

117543964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448336-T-G

http://identifiers.org/hco/10/GRCh38#117543972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59448348-C-A

117543972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448348-C-T

117543997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448373-G-A

117543997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448373-G-T

http://identifiers.org/hco/10/GRCh38#117543998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59448374-C-A

http://identifiers.org/hco/10/GRCh38#117544127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59448496-C-A

117544168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448537-T-G

117544216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448576-T-C

117544226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448586-T-C

117544226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448586-T-G

117544230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448590-T-C

117544230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448590-T-G

http://identifiers.org/hco/10/GRCh38#117544399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59448815-C-A

http://identifiers.org/hco/10/GRCh38#117544572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59448986-C-A

117544572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59448986-C-T

117544584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59448997-A-G

117544584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59448997-A-T

117544810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59449251-G-A

117544810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59449251-G-T

http://identifiers.org/hco/10/GRCh38#117545032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59449464-C-A

117545032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59449464-C-T

http://identifiers.org/hco/10/GRCh38#117545052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#59449481-C-A

117545052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18511
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59449481-C-T