http://identifiers.org/hco/5/GRCh38#54977929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113354568-C-A

54977963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113354533-C-T

54978013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113354483-C-T

54978058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113354438-C-T

54978059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113354437-T-C

54978285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113354210-T-C

54978291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113354209-T-C

54978653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353895-T-A

54978653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353895-T-C

54978666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353867-C-T

54978813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353756-G-A

54978813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353756-G-T

http://identifiers.org/hco/5/GRCh38#54978828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113353743-C-A

http://identifiers.org/hco/5/GRCh38#54978903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113353685-A-C

54978964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353621-T-A

54978999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353593-G-C

54978999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353593-G-T

http://identifiers.org/hco/5/GRCh38#54979050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113353554-A-C

54979050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3 prime UTR variant
orthologous variants: 113353554-A-T

54979102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 113353487-T-C

54979425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 113353182-C-T

54979553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113353054-T-A

54979607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113353004-G-A

54979641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352971-C-T

54979738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352879-T-C

54979791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352813-A-T

54979811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352793-T-C

54980035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352585-G-A

54980035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352585-G-C

http://identifiers.org/hco/5/GRCh38#54980061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113352562-C-A

54980284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352296-C-T

http://identifiers.org/hco/5/GRCh38#54980404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113352175-C-A

54980404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352175-C-G

54980615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113352016-C-T

54980834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350803-A-G

54980977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350685-G-A

54981608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350325-T-C

http://identifiers.org/hco/5/GRCh38#54981768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113350184-C-A

http://identifiers.org/hco/5/GRCh38#54981870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113350093-C-A

54981870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350093-C-T

http://identifiers.org/hco/5/GRCh38#54981871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113350092-C-A

54981871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350092-C-T

54981911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350060-T-A

54981911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350060-T-C

54981919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113350059-T-C

54982180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349859-C-T

54982215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349824-G-A

54982258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349783-T-A

54982258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349783-T-C

54982488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349288-C-T

54982496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349280-G-C

54982734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113349078-T-G

54982971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113348867-T-C

54983373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113348508-T-C

54983428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113348463-A-G

54983428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113348463-A-T

54983785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113348130-G-A

54983832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113348082-A-T

54984099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113347777-T-A

54984310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113347566-A-G

54984317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113347559-G-A

54984617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113347257-A-T

54984647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113347227-T-G

54984841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113347030-T-A

54984890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346981-C-T

54984957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346913-T-C

54984983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346885-A-G

54985101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346779-A-G

54985140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346752-A-G

http://identifiers.org/hco/5/GRCh38#54985145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113346747-A-C

54985145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346747-A-T

54985153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346739-T-A

54985206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113346686-T-G

54985252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113346640-T-A

54985429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 113346463-T-G

http://identifiers.org/hco/5/GRCh38#54985897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113345987-C-A

54985897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113345987-C-G

54985897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 113345987-C-T

http://identifiers.org/hco/5/GRCh38#54985968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113345917-C-A

54986000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113345889-G-A

54986039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113345801-G-T

54986439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113345388-G-C

54986476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113345353-A-G

54986712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113345094-A-G

54986746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113345065-C-T

http://identifiers.org/hco/5/GRCh38#54986776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113345029-A-C

54986886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113344930-G-A

54987447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113343108-A-G

54988178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113342407-T-C

http://identifiers.org/hco/5/GRCh38#54988271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113342326-C-A

54988323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113342269-G-A

54988324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113342268-T-A

54988333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113342262-A-G

54988357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113342238-C-T

54988503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113342106-T-C

54988829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341807-A-G

54988850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341786-A-T

54988990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341649-T-C

54989009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341627-T-G

54989106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341539-A-G

54989178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341511-C-T

54989244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341463-A-G

54989262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341444-G-C

54989383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341340-T-C

54989418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341324-T-C

54989485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341278-G-A

54989580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113341031-G-A

54989950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113340509-G-A

54990152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113340276-C-T

54990303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113340125-G-T

54990323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113340112-G-A

54990331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113340104-T-A

54990347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113340088-T-C

54990443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113339575-A-G

54990448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113339570-G-A

54990661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113339402-A-G

54990752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113339330-A-G

54990929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113339162-C-T

http://identifiers.org/hco/5/GRCh38#54991261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113338828-C-A

54991513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113338592-C-T

54991560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113338488-C-G

54991560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113338488-C-T

54991634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113338408-C-T

54992070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113338031-G-A

54992070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113338031-G-C

54992163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337949-C-T

54992294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337835-A-G

http://identifiers.org/hco/5/GRCh38#54993441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113337473-C-A

54993441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337473-C-T

54993456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337458-T-C

54993480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337436-A-G

54993535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 113337386-A-G

54993550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113337370-T-C

54993595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113337325-C-T

http://identifiers.org/hco/5/GRCh38#54993624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113337296-C-A

54993624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113337296-C-T

http://identifiers.org/hco/5/GRCh38#54993633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113337287-A-C

http://identifiers.org/hco/5/GRCh38#54993642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113337278-C-A

54993673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 113337273-G-T

http://identifiers.org/hco/5/GRCh38#54993680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113337266-A-C

54993680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 113337266-A-G

54993875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337090-G-A

54993884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337081-C-G

54993914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337056-C-G

54993915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337055-T-C

54993938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337031-C-T

54993971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337001-G-A

54993971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113337001-G-C

54993994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113336978-C-G

54993994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113336978-C-T

54994346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335689-T-C

54994408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335630-A-T

54994505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335550-G-A

54994568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335452-T-G

54994679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335289-G-A

54994808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335161-G-T

54995273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113335025-A-G

54995533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113334775-C-T

54995945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113334685-A-G

54996520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113334090-A-T

54997241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333398-G-A

54997241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333398-G-C

54997362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333284-C-T

54997363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333283-A-G

http://identifiers.org/hco/5/GRCh38#54997515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113333156-C-A

54997515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333156-C-T

54997589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333083-G-C

54997626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113333049-G-C

http://identifiers.org/hco/5/GRCh38#54997702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113332971-C-A

54997779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332900-G-A

54997801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332879-G-A

http://identifiers.org/hco/5/GRCh38#54997834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113332847-C-A

54997834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332847-C-T

54997879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332805-G-A

54997879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332805-G-C

http://identifiers.org/hco/5/GRCh38#54998093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113332629-C-A

54998336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332395-G-A

54998353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332378-T-C

54998357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332374-A-G

54998387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332345-C-T

54998420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332323-A-T

54998444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332296-T-A

54998982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113332103-T-A

55003233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113331827-A-G

55003233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113331827-A-T

55003457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113331604-C-T

55003620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113331447-A-G

55003787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113331281-C-T

55004143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330936-C-T

55004276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330843-G-A

55004326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330793-A-T

55004331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330788-G-A

55004349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330727-C-T

http://identifiers.org/hco/5/GRCh38#55004411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113330665-C-A

55004411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330665-C-T

55004480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330639-A-G

55004584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330535-A-G

55004654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330467-G-A

55004655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330466-T-C

55004689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330434-G-T

55004800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330302-T-C

55004800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330302-T-G

55004805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330276-G-A

55004872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330211-G-A

55004983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113330100-T-C

55005200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113329877-T-A

55005200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113329877-T-C

55005204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113329864-G-A

55019205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113326683-C-T

55019534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113326205-G-T

http://identifiers.org/hco/5/GRCh38#55019568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113324249-A-C

55019708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113324114-T-C

55019809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113322176-G-A

55019809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113322176-G-T

55019974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321991-G-T

55020133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321836-G-A

http://identifiers.org/hco/5/GRCh38#55020211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113321768-C-A

55020230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321750-A-G

55020537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321461-G-T

55020544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321454-C-T

55020678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321294-G-C

55020682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321290-T-A

55020760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321210-T-C

55020835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113321102-C-T

55020946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320992-G-C

55020966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320979-G-C

55021014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320472-G-A

http://identifiers.org/hco/5/GRCh38#55021018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113320468-C-A

55021129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320376-C-T

http://identifiers.org/hco/5/GRCh38#55021145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113320360-C-A

55021145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320360-C-T

55021166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320339-T-C

http://identifiers.org/hco/5/GRCh38#55021214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113320296-C-A

55021286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113320227-G-T

55021464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 113320065-A-G

http://identifiers.org/hco/5/GRCh38#55021502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113320031-C-A

55021534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319999-G-A

55021563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319975-C-T

55021568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319969-A-G

http://identifiers.org/hco/5/GRCh38#55021837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113319694-A-C

55021840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319691-C-T

55021925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319607-T-C

55022130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319408-C-T

55022200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319341-C-T

55022317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319236-C-T

55022438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319141-G-A

55022459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319120-G-A

55022485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319094-A-T

55022496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319083-A-G

55022515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319063-A-G

55022557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3466
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 113319022-T-C