http://identifiers.org/hco/1/GRCh38#97933539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118341876-A-C

97933632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118341782-A-T

97933676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118341738-G-T

http://identifiers.org/hco/1/GRCh38#97933744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118341670-C-A

97933855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118341559-A-G

97934152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118341256-G-T

97934177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118341231-A-G

97934177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118341231-A-T

97934198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118341210-A-G

http://identifiers.org/hco/1/GRCh38#97934242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118341168-C-A

97934255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118341154-A-G

97934255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118341154-A-T

http://identifiers.org/hco/1/GRCh38#97934286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118341130-C-A

97934286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118341130-C-T

97934290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118341126-T-G

http://identifiers.org/hco/1/GRCh38#97934375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118341059-C-A

97934422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118341011-G-A

97934843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118340618-T-A

97934843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118340618-T-C

97935476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118340030-G-T

http://identifiers.org/hco/1/GRCh38#97935513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118340000-C-A

97935711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118339713-A-T

97935716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118339708-G-C

97935778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118339660-T-C

97936723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118337650-C-T

97936899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118337327-T-G

http://identifiers.org/hco/1/GRCh38#97937101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118337114-A-C

97937129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118337092-A-G

97937139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118337082-A-G

97937266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336914-G-T

97937309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336879-G-T

97937371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336849-G-A

97937371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336849-G-C

97937505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336382-C-T

97937873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336078-T-G

97937897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118336053-T-C

97938000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118335976-A-G

97939729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118335533-G-A

97939887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118335390-A-G

97940028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118335111-T-C

97940032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118335107-T-A

97940032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118335107-T-C

97940504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118334736-A-G

97941016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118334111-C-G

97941016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118334111-C-T

97941225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333921-T-G

97941305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333844-T-G

97941369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333784-A-G

97941369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333784-A-T

97941488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333664-G-A

97941488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333664-G-C

97941488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333664-G-T

97941778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333441-C-T

97941787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333433-A-T

97941818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333402-A-G

97942095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118333067-A-G

97942191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332970-T-C

97942218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332926-G-A

97942218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332926-G-C

97942218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332926-G-T

97942307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332852-C-T

97942471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332713-T-C

97942680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332512-C-G

97942680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332512-C-T

97942803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332369-C-T

97942920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332248-G-A

http://identifiers.org/hco/1/GRCh38#97942955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118332213-C-A

97942955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332213-C-T

97943121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118332035-G-A

http://identifiers.org/hco/1/GRCh38#97943265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118331733-A-C

97943289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118331690-C-G

http://identifiers.org/hco/1/GRCh38#97943569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118331437-C-A

97943713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118331295-A-T

97943821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118331158-T-G

http://identifiers.org/hco/1/GRCh38#97943959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118331017-A-C

97943959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118331017-A-G

97944007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118330969-T-G

97944398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118330912-G-A

97946515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118330285-T-C

97946515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118330285-T-G

97947115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118329684-G-A

97947258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118329550-G-A

97947567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118329103-G-T

97947599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118329071-A-G

97947850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118328824-G-A

97947881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118328794-G-T

97948083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118328564-A-G

97948132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118328516-A-G

97948807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118327755-T-C

97948848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118327715-G-A

97948912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118327647-G-A

97948937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118327455-T-C

97948964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118327426-G-A

97948994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118327381-A-G

97949382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118326987-T-G

97949551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118326851-T-A

97949551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118326851-T-C

97949988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325989-A-G

97950051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325929-C-T

97950130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325852-C-T

97950133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325849-G-T

97950252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325764-G-A

97950252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325764-G-T

97950396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325654-A-T

97950490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325560-G-C

97950493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325557-T-C

http://identifiers.org/hco/1/GRCh38#97950670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118325388-C-A

97950734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325321-T-C

97950759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325296-C-T

97950799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118325258-C-G

97951361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118324391-C-T

97951967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118323823-G-A

97951967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118323823-G-C

http://identifiers.org/hco/1/GRCh38#97952085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118323700-C-A

http://identifiers.org/hco/1/GRCh38#97952254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118323523-C-A

97952289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118323482-G-A

97952447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118323342-C-T

http://identifiers.org/hco/1/GRCh38#97952481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118323316-A-C

97952481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118323316-A-G

97966291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118317475-T-G

97966340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118317426-T-G

97966414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118317368-T-A

97966414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118317368-T-C

97966414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118317368-T-G

97966419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118317363-A-G

97967553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118316755-A-G

97967895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118316425-T-C

97968124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118316194-A-G

97968136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118316183-T-G

97968440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118315886-T-C

97968486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118314967-A-G

97968532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118314931-C-G

97968662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118314781-G-A

97968690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118314751-A-G

http://identifiers.org/hco/1/GRCh38#97968734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118314700-C-A

97968738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118314696-T-C

97968765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118314670-G-T

http://identifiers.org/hco/1/GRCh38#97968767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118314668-A-C

97968891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118314544-A-G

http://identifiers.org/hco/1/GRCh38#97969170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118314268-A-C

97969439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118314013-G-A

97969952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118313811-T-G

97970443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118313325-A-T

97970476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118313292-C-T

97970626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118313114-G-T

97970766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312967-G-A

97970766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312967-G-T

97970869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312873-A-G

97971014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312755-A-T

97972000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312623-T-G

97972079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312542-G-C

97972079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312542-G-T

97972103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312520-C-T

http://identifiers.org/hco/1/GRCh38#97972122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118312471-C-A

97972122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312471-C-T

97972130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312455-G-T

97972386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312214-C-T

http://identifiers.org/hco/1/GRCh38#97972616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118312012-A-C

97972616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118312012-A-G

97972749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311890-A-T

97972800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311838-G-A

97972809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311828-A-T

97972824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311813-C-T

97972935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311699-T-C

97973020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311614-G-A

97973020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311614-G-T

97973156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118311491-G-A

97973369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310729-C-T

97973378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310719-C-T

97973390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310707-T-G

97973593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310512-A-G

97973593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310512-A-T

97973846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310270-G-T

97973945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310171-A-G

http://identifiers.org/hco/1/GRCh38#97973953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118310163-C-A

97974010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118310119-A-G

97974257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118309489-G-A

97974817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118307988-T-A

http://identifiers.org/hco/1/GRCh38#97974991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118307888-C-A

97974991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118307888-C-T

97975588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118307273-A-T

97975636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118307225-A-T

97975740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118307169-A-T

97975973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118306858-C-T

97976194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118306652-T-C

97976214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118306632-T-C

97976279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118306548-T-C

97976717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118306108-T-C

97976961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118305868-T-C

97977171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118305655-T-C

97977171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118305655-T-G

97977328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118305496-A-G

97977544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118305281-T-A

97977551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118305274-T-C

http://identifiers.org/hco/1/GRCh38#97977883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118304942-C-A

97978448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304681-G-A

97978451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304678-T-C

97978709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304452-C-T

97978850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304359-C-T

97978856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118304353-G-A

97979203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303900-T-C

http://identifiers.org/hco/1/GRCh38#97979220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118303882-C-A

97979220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303882-C-T

97979312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118303791-G-A

97979329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303774-A-T

97979338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303765-A-G

97979387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303300-T-C

97979484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303204-G-T

97979515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118303173-T-C

97979697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302991-A-G

97979819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302863-T-C

97979885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302786-G-A

97979968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302712-T-C

97980416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302034-C-T

97980451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118302001-T-A

97980499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118301942-A-G

97980627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118301836-A-G

http://identifiers.org/hco/1/GRCh38#97980845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118301617-C-A

97980845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118301617-C-T

97981228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118301165-C-T

97981239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118301157-T-G

97981279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118301118-A-G

97982164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118299049-C-T

97982225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298989-G-A

97982261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298963-T-C

97982264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298960-G-C

97982265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298959-T-A

97982294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298956-A-G

97982888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298416-A-G

97983024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298283-G-T

97983215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298209-C-T

97983276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298149-A-G

97983448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118298001-T-G

97985540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295948-C-T

http://identifiers.org/hco/1/GRCh38#97985599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118295890-C-A

97985599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295890-C-T

http://identifiers.org/hco/1/GRCh38#97985715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118295775-C-A

97985718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295772-A-G

97985956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295558-T-C

97985988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295518-T-C

97985994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295512-G-A

97986438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295072-G-A

97986440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118295070-G-A

http://identifiers.org/hco/1/GRCh38#97986618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118294621-C-A

97986618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118294621-C-G

97986620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118294619-T-G

97986775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294462-T-C

http://identifiers.org/hco/1/GRCh38#97986778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118294459-C-A

97986778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294459-C-T

97986813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294395-A-G

http://identifiers.org/hco/1/GRCh38#97986819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118294389-C-A

97986819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294389-C-G

97986819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294389-C-T

97986855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294353-C-T

97986858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294350-A-G

97986873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294335-G-A

97986902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294298-A-G

http://identifiers.org/hco/1/GRCh38#97986967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118294247-C-A

http://identifiers.org/hco/1/GRCh38#97986977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118294237-C-A

97986977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294237-C-G

97987056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118294183-G-T

http://identifiers.org/hco/1/GRCh38#97987172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118294079-C-A

97987363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293908-C-T

97987366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293905-A-G

97987377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293894-T-A

97987377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293894-T-C

97987377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293894-T-G

http://identifiers.org/hco/1/GRCh38#97987384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293887-C-A

97987384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293887-C-T

97987387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293886-A-G

97987390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293883-T-C

http://identifiers.org/hco/1/GRCh38#97987406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293866-C-A

97987406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293866-C-G

97987464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293777-G-C

97987509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293643-T-A

97987509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293643-T-C

97987515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293637-T-A

97987515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293637-T-C

97987534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293618-T-C

http://identifiers.org/hco/1/GRCh38#97987664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293487-C-A

97987692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293460-T-C

97987725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293432-C-T

97987813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293355-A-G

97987836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293342-A-G

97987836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293342-A-T

http://identifiers.org/hco/1/GRCh38#97987850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293328-C-A

97987850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293328-C-T

97987870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293289-T-C

97987926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293233-C-T

http://identifiers.org/hco/1/GRCh38#97987932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293227-C-A

97987989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293174-C-G

97988068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293100-G-T

http://identifiers.org/hco/1/GRCh38#97988089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293079-C-A

97988089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293079-C-G

http://identifiers.org/hco/1/GRCh38#97988096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118293073-C-A

97988100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293069-T-C

97988122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293054-G-A

97988122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293054-G-T

97988124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293052-A-G

97988148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118293001-T-C

97988165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292963-A-G

97988169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292959-G-A

http://identifiers.org/hco/1/GRCh38#97988171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118292957-C-A

97988171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292957-C-T

97988176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292952-T-C

97988201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292850-T-C

97988207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292844-T-A

97988215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292837-G-A

97988215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292837-G-T

97988286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292766-G-T

97988306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292745-G-A

http://identifiers.org/hco/1/GRCh38#97988369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118292683-C-A

97988630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292442-A-G

97988732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118292346-A-T

97989140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118290405-T-C

http://identifiers.org/hco/1/GRCh38#97989290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118290245-A-C

97989290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118290245-A-T

97989303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118290233-C-T

97989368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118290177-A-G

97991252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118288262-T-C

97991253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118288261-T-A

97991539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287956-C-T

97991886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118287630-A-G

http://identifiers.org/hco/1/GRCh38#97991979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118287534-C-A

97992119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286554-C-T

97992217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286464-A-T

97992317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286282-G-C

http://identifiers.org/hco/1/GRCh38#97992369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118286231-C-A

97992398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286202-T-C

97992424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118286176-T-C

97992624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285980-C-G

97992728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285876-A-G

http://identifiers.org/hco/1/GRCh38#97992734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118285871-C-A

http://identifiers.org/hco/1/GRCh38#97992804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118285793-C-A

97992818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285774-T-C

97992824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285757-A-G

97992955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285381-T-A

97992977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285359-G-A

97993146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285190-C-G

97993171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285165-A-G

http://identifiers.org/hco/1/GRCh38#97993173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118285163-A-C

97993173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285163-A-T

97993186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285150-G-A

97993186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285150-G-C

http://identifiers.org/hco/1/GRCh38#97993187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118285149-A-C

97993203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285133-G-A

97993203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285133-G-T

97993277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118285057-A-G

97993447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284931-A-T

97993724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284662-G-A

97993724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284662-G-T

97993885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284497-G-A

97993885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284497-G-T

http://identifiers.org/hco/1/GRCh38#97993979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118284404-A-C

97994088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284293-G-A

97994139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284244-G-A

97994139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118284244-G-T

97994647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283445-A-T

97994655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283437-G-A

97994785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118283314-T-C

http://identifiers.org/hco/1/GRCh38#97994898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118283214-C-A

http://identifiers.org/hco/1/GRCh38#97994908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118283204-C-A

97994908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118283204-C-T

97994938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118283175-G-A

97994951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118283162-A-G

97995269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118282829-T-C

97997045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281261-G-A

97997057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281249-T-A

97997120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281197-A-G

97997204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281119-G-A

97997204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281119-G-C

97997285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281039-A-G

97997311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118281019-A-G

97997548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280783-G-T

http://identifiers.org/hco/1/GRCh38#97997631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118280693-A-C

97997699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280638-C-G

97997699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280638-C-T

97997886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280504-A-G

97998086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280317-A-G

97998129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280273-A-G

97998177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280225-T-C

97998254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280146-G-T

97998258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118280142-A-G

97998395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279987-T-C

97998401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279981-A-G

97998405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118279977-A-T

97998719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278829-T-C

97998721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278827-T-C

97998788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278772-G-T

97998855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278716-T-G

97998929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278647-T-A

97998930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278646-C-T

97998995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278580-T-G

97999037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278527-G-A

97999151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278410-G-T

97999267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278299-G-A

97999273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278294-T-C

http://identifiers.org/hco/1/GRCh38#97999337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118278233-A-C

97999341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278229-T-C

97999370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278196-T-C

97999437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278130-C-T

97999472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278087-C-T

97999526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278040-T-C

97999555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118278009-G-T

97999944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277657-G-T

98000038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277564-A-G

98000084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277523-T-C

98000195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277421-T-A

98000207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277409-T-C

98000483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277134-T-C

98000775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277063-G-A

98000810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118277029-T-C

98000987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276866-T-C

98001077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276776-T-C

98001177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276675-A-G

98001228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118276631-A-G

98001693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118275227-T-A

98001693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118275227-T-C

98001761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118275152-C-G

98001938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274987-C-G

98001938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274987-C-T

98001988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274938-G-T

98002113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118274816-A-G

98003032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273090-G-T

98003036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118273086-T-A

98003164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272974-T-A

98003164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272974-T-C

98003331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272541-T-C

98003616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272250-G-A

http://identifiers.org/hco/1/GRCh38#98003711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118272166-C-A

98003711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272166-C-G

98003729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272148-T-C

98003753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272124-T-C

98003855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118272021-C-T

98003898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271980-A-G

98003946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271932-C-T

98004061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271816-T-C

98004076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271801-T-C

98004156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271716-A-G

98004194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271676-G-A

98004291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271581-T-G

98004323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271549-G-A

98004446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118271297-A-T

http://identifiers.org/hco/1/GRCh38#98004448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118271295-C-A

http://identifiers.org/hco/1/GRCh38#98004899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118271033-A-C

98005122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118270854-A-T

98005147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118270838-A-T

http://identifiers.org/hco/1/GRCh38#98005272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118270703-C-A

98005318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118270657-G-A

98005318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118270657-G-T

98005329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118270646-C-T

98005600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118270406-A-G

98005637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118270370-C-T

98005661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118270337-G-A

98005776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118270222-T-A

98005952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118270053-C-G

98005952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118270053-C-T

98005962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118270044-T-A

98006035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269976-C-T

98006053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269958-C-T

98006147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269865-T-C

98006238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269780-A-G

98006294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269736-T-G

98006715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269373-G-A

98006752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269336-T-C

98006790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269305-G-A

98006813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269292-G-A

98007079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269066-A-G

98007105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269040-T-C

98007108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118269037-T-C

98007375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118268748-G-A

98007399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118268724-C-T

98007455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118268673-A-G

98007585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118268546-G-T

http://identifiers.org/hco/1/GRCh38#98008549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118267779-A-C

http://identifiers.org/hco/1/GRCh38#98008561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118267738-C-A

98008591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267714-A-G

98008839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267466-G-A

98008848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267457-T-C

http://identifiers.org/hco/1/GRCh38#98008883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118267403-C-A

98009040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118267243-G-T

http://identifiers.org/hco/1/GRCh38#98009134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118267173-C-A

98009384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266927-A-G

98009421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266894-G-A

98009531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266781-T-C

http://identifiers.org/hco/1/GRCh38#98009624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118266687-C-A

98009708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266612-C-T

98009789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266524-A-G

98009789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266524-A-T

98010179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266126-G-A

98010298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118266002-A-G

98010548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265717-G-A

98010584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265686-A-G

98010882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118265359-A-G

98011235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118264984-C-G

98011240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118264979-C-T

98011435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

98012106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118263169-C-T

http://identifiers.org/hco/1/GRCh38#98012117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118263162-C-A

98012117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118263162-C-T

98014274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118262513-G-A

98014489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118262331-T-C

98014573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118262246-C-T

98014685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118262137-G-A

98014741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118262097-G-A

98015043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118261851-C-G

98015318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118261602-T-C

98015397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118261517-C-T

98015412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118261502-T-C

98016240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118260713-A-T

98017006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118257449-A-G

98017041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118257415-T-G

98017466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256784-A-G

98017627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256654-G-A

98017627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256654-G-T

98018167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256144-T-A

98018167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256144-T-G

98018203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256113-G-A

98018246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118256064-T-C

98018437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255875-A-T

98018734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255575-T-G

98019307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255203-C-G

98019378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255131-G-A

98019378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118255131-G-T

98019519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254996-A-G

98019690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254832-A-G

http://identifiers.org/hco/1/GRCh38#98019754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118254792-A-C

98019869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118254665-C-T

98019897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254636-T-C

98019938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254595-C-T

98019981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254552-T-G

98020054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254479-T-C

98020054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254479-T-G

98020244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254391-C-T

98020454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254359-A-G

98020840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118254053-A-G

98021200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118253601-T-A

98021200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118253601-T-C

98021423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118253382-T-C

http://identifiers.org/hco/1/GRCh38#98021795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118253004-C-A

98021909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252921-A-T

98021913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252917-G-A

98021968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252871-C-T

http://identifiers.org/hco/1/GRCh38#98022215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118252691-A-C

98022523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252396-A-G

98022705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118252228-T-C

http://identifiers.org/hco/1/GRCh38#98022908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118251979-C-A

98023168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251788-T-C

98023245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251699-T-A

98023585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251331-A-G

98023773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118251141-G-T

98023957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118250965-T-C

98024248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118250649-G-A

98024248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118250649-G-T

98024364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118250537-T-C

98024728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118250176-T-A

98024868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118250048-T-A

98024930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249983-G-T

98024951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249950-A-G

98025017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249886-T-G

98025171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249739-T-A

98025288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249618-A-G

98025335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249573-T-G

http://identifiers.org/hco/1/GRCh38#98025438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118249480-C-A

98025689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249209-T-C

98025700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118249198-T-C

98025926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248821-C-T

98025964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248783-T-C

98026011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248737-C-G

98026142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248610-T-C

98026246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248516-T-G

98026477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248296-T-C

98026627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248147-A-G

98026713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118248064-G-A

98026930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247659-G-C

98026995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247550-C-T

98027040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247508-A-G

98027096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247455-T-A

98027132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247419-T-G

98027251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247318-T-A

98027301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247257-C-G

98027355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247202-G-A

98027413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247145-C-T

98027568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247068-G-A

98027594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247046-C-T

http://identifiers.org/hco/1/GRCh38#98027639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118247003-A-C

98027641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118247001-G-A

98027689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246954-C-T

98027710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246938-T-C

98027714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246934-T-A

98027714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246934-T-C

98028021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246636-T-C

98028021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246636-T-G

98028134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246533-T-A

98028143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246524-T-C

98028229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246412-G-A

98028370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246247-T-C

http://identifiers.org/hco/1/GRCh38#98028520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118246094-C-A

98028529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118246085-G-A

98028732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245885-A-G

98028776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245855-T-A

98028880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245519-C-G

98029291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245109-G-A

98029300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118245100-A-G

98029570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118244543-G-T

98029733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118244407-A-G

98029812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118244329-C-T

98029917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118244239-T-C

98030075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118244078-T-C

98030090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118244064-T-C

98030222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243949-T-A

98030222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243949-T-C

98030271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243896-T-G

98030343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243824-T-C

98030401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243766-G-A

98030445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243722-C-T

98030488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243679-T-C

http://identifiers.org/hco/1/GRCh38#98030576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118243588-C-A

98030637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243527-C-T

98030670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243494-A-G

98030733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118243431-T-A

98031237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118242766-C-T

98031338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118242678-A-G

98031909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118241540-A-G

98031933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118241515-A-G

98032281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118241170-T-C

98032780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118241030-G-A

98032780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118241030-G-T

98032862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240954-A-G

98032869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240942-A-G

98032875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240936-T-A

98032881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240930-A-T

98032995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240830-A-G

98033041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240784-C-T

98033086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240740-G-A

98033183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240643-A-T

98033315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240515-G-T

98033366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240463-A-G

98033434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240399-T-C

98033545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240147-G-A

98033614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118240076-T-C

98033801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239951-A-G

98033807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239945-C-T

98033819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239933-A-G

http://identifiers.org/hco/1/GRCh38#98033862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118239894-C-A

98033862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239894-C-G

98033862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239894-C-T

98033868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239888-A-G

http://identifiers.org/hco/1/GRCh38#98033869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118239887-C-A

98033912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239854-T-C

98033966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239804-T-G

98033999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239772-A-G

98034024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239747-T-C

http://identifiers.org/hco/1/GRCh38#98034042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118239729-A-C

http://identifiers.org/hco/1/GRCh38#98034316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118239591-A-C

98034340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239567-A-G

98034391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239524-G-A

98034392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239523-G-A

98034593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239330-T-A

98034655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239279-T-C

98034777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118239155-C-T

98034790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118239087-T-G

98034889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118238980-T-G

98035372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118238072-C-T

98035420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118238026-T-C

98035430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118238016-A-G

98035582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118237868-T-C

98035582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118237868-T-G

98036122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118237333-T-C

98036521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118236956-A-G

98036666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118236905-A-G

http://identifiers.org/hco/1/GRCh38#98036866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118236830-A-C

98037030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118236730-C-T

98037074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118236686-A-G

98037457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118236131-G-A

98037744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118235852-T-G

98037837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118235762-T-C

98038069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118235553-T-A

98038075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118235548-G-T

http://identifiers.org/hco/1/GRCh38#98038271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118235339-C-A

98038271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118235339-C-G

98038800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234776-G-A

98039226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234449-A-G

98039368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234309-T-A

98039473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234203-T-C

98039506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118234175-A-G

98039815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233894-T-C

98039861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233838-A-G

98039878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118233821-C-T

http://identifiers.org/hco/1/GRCh38#98040126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118233546-C-A

http://identifiers.org/hco/1/GRCh38#98040549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118233086-C-A

http://identifiers.org/hco/1/GRCh38#98040594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118233033-A-C

98040754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118232874-G-A

98040808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118232820-G-A

98040945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118232678-T-C

98041382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118232362-T-C

98041531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118232216-A-G

98041573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118232175-A-G

98042140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118231536-A-G

98042181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118231493-A-T

http://identifiers.org/hco/1/GRCh38#98042302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118231413-C-A

98042575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118231161-A-G

98042904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230789-G-A

98043114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230562-G-C

http://identifiers.org/hco/1/GRCh38#98043262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118230405-C-A

98043262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230405-C-G

http://identifiers.org/hco/1/GRCh38#98043351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118230324-C-A

98043351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230324-C-G

98043357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230318-G-A

98043410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230265-T-C

98043415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230260-G-C

98043536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230126-T-C

98043537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118230125-G-A

98043816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229839-A-G

http://identifiers.org/hco/1/GRCh38#98043882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118229746-C-A

98043882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229746-C-T

98043950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229689-G-A

http://identifiers.org/hco/1/GRCh38#98044136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118229505-A-C

98044303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229342-G-A

98044361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229284-G-T

98044447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229203-G-T

98044474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229189-T-C

98044627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229035-G-A

98044627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229035-G-T

98044636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229026-G-A

98044637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229025-A-G

98044640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229022-G-A

98044640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229022-G-C

98044640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118229022-G-T

98044824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228856-G-A

98044824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228856-G-C

98044835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228845-T-G

98044838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228842-G-T

98044883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228802-G-T

http://identifiers.org/hco/1/GRCh38#98044892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228793-C-A

98044892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228793-C-T

http://identifiers.org/hco/1/GRCh38#98044978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228713-C-A

98045035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228658-C-T

98045052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228639-G-A

98045052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228639-G-T

98045088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228603-A-G

98045172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228548-G-T

98045221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228499-C-T

98045241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228478-G-A

http://identifiers.org/hco/1/GRCh38#98045295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228424-C-A

http://identifiers.org/hco/1/GRCh38#98045365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228354-C-A

98045423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228296-A-G

http://identifiers.org/hco/1/GRCh38#98045475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228244-C-A

98045475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228244-C-T

http://identifiers.org/hco/1/GRCh38#98045543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228176-C-A

98045543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118228176-C-T

http://identifiers.org/hco/1/GRCh38#98045566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228153-C-A

http://identifiers.org/hco/1/GRCh38#98045642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118228075-A-C

http://identifiers.org/hco/1/GRCh38#98045866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118227810-C-A

98045866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227810-C-T

http://identifiers.org/hco/1/GRCh38#98045909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118227746-C-A

98045909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227746-C-T

98045934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227711-G-T

98046225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118227436-G-A

http://identifiers.org/hco/1/GRCh38#98046238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118227423-C-A

98046284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118227374-G-A

98046284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118227374-G-C

http://identifiers.org/hco/1/GRCh38#98046352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118227306-C-A

98046352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118227306-C-G

98046352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118227306-C-T

98046448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227202-T-C

98046464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227184-G-T

98046495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118227162-A-G

98046539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non coding transcript exon variant
orthologous variants: 118227118-T-C

98046660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118226993-T-G

98046703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118226950-T-C

http://identifiers.org/hco/1/GRCh38#98046722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118226930-C-A

98046722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118226930-C-T

98046926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118226736-T-C

98047576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118226101-C-G

98047608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118226068-C-T

98047610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118226066-G-A

98047902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118225790-A-T

98048100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118225592-C-T

98048265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118225436-A-G

98048524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118225109-T-C

98048619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118225013-C-T

http://identifiers.org/hco/1/GRCh38#98048967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#118224660-A-C

98049064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224536-C-T

98049224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224369-A-G

98049303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118224290-C-T

http://identifiers.org/hco/1/GRCh38#98049526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#118224064-C-A

98049526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118224064-C-T

98049546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118224044-G-A

98049594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42871
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 118223996-G-A