99638501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57575177-G-T

http://identifiers.org/hco/3/GRCh38#99638909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57574758-C-A

99639005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57574646-A-G

99640140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57573519-A-G

http://identifiers.org/hco/3/GRCh38#99640277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57573382-C-A

99640588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57573091-A-G

99640826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572855-G-A

99640912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572796-C-G

99641002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572718-G-A

99641064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572650-T-C

99641145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572575-G-C

99641154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572561-A-T

99641248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572468-C-T

99641426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572280-T-A

99641426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57572280-T-C

99641848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571940-G-A

http://identifiers.org/hco/3/GRCh38#99641859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57571931-A-C

99641859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571931-A-G

99642040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571756-C-T

http://identifiers.org/hco/3/GRCh38#99642427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57571394-C-A

99642427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571394-C-T

99642533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571278-A-G

99642534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571277-T-A

99642534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571277-T-C

99642546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57571265-T-C

http://identifiers.org/hco/3/GRCh38#99642730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57571107-A-C

99643136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57570712-G-A

99643188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57570662-G-A

99643286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57570578-C-T

99643570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57570337-T-G

99643592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57570332-A-G

99643750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57570182-T-C

http://identifiers.org/hco/3/GRCh38#99644050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57569969-C-A

99644050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57569969-C-T

http://identifiers.org/hco/3/GRCh38#99644119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57569896-C-A

99644335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57569707-G-A

99644372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57569670-T-C

99644380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57569662-A-T

99644560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57569481-T-A

99645070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57568992-G-A

99645264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57568806-A-G

99645273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57568797-A-G

99646168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57567882-A-G

99646200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57567850-A-G

99646442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57567589-G-A

99646636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57567400-A-G

99647189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565921-C-T

99647205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565905-G-A

99647374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565719-A-G

99647412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565681-C-T

99647551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565501-T-C

99647666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565379-C-T

99647708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565339-T-C

99647808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565237-T-C

99647960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57565091-G-A

99648473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57564449-T-A

http://identifiers.org/hco/3/GRCh38#99648475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57564448-A-C

99648475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57564448-A-T

99648766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57564167-G-T

http://identifiers.org/hco/3/GRCh38#99648859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57564077-A-C

99649085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57563885-T-C

99649124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57563847-T-C

99649214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57563761-C-G

http://identifiers.org/hco/3/GRCh38#99649221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57563754-C-A

99649357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57563639-T-A

99649395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57563603-G-A

99649653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57563351-A-G

http://identifiers.org/hco/3/GRCh38#99649726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57563250-C-A

99649863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57562835-A-G

99649866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57562832-A-G

99649916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57562781-G-C

99649969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57562724-A-G

99650019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57562674-T-G

99650263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57562419-C-G

http://identifiers.org/hco/3/GRCh38#99651693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57560573-C-A

99651750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57560516-G-A

99651750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57560516-G-T

99651985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57560291-T-G

99651991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57560285-G-A

http://identifiers.org/hco/3/GRCh38#99652188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57559530-A-C

99652276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57559446-T-C

99652329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57559386-C-T

99652459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57559263-A-G

99652535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57559197-C-T

99652565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57559175-A-G

99654960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57558516-A-T

99655179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57558297-G-C

99655249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57558227-A-G

99655489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57558008-T-C

99655886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57557641-G-T

99655889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57557638-C-G

99655889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57557638-C-T

99656081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57557459-T-C

99656257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57557282-C-T

http://identifiers.org/hco/3/GRCh38#99656328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57557219-A-C

99656484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57557051-T-A

99656590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556950-A-T

99656956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556609-A-T

99657010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556537-C-T

99657119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556430-T-A

99657275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556263-A-G

99657364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556214-A-T

99657373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556205-T-G

99657424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556157-A-G

99657454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57556127-G-A

99657790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57555798-G-C

99659200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57554551-T-C

99659567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57554221-T-C

99659597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57554191-T-G

99659749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57554034-G-T

99660232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57553558-A-G

99660742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57553085-G-C

99661328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57552269-A-G

99662653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57551863-C-T

99662754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57551768-T-C

99662754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57551768-T-G

99663387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57550008-G-A

99663561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57549827-C-T

99663955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57549452-G-T

99663962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57549445-C-G

99664126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57549270-G-T

99664274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57549135-C-T

99664408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548999-T-C

http://identifiers.org/hco/3/GRCh38#99664550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57548917-C-A

99664584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548884-T-C

99664687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548790-G-T

99664708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548778-G-A

99665006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548483-C-T

99665045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548444-C-T

99665112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548376-G-A

99665119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548369-T-C

99665126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548362-G-A

99665195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548296-G-C

99665370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548129-T-C

99665383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548115-A-G

99665403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57548095-T-C

99665508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57547990-G-A

99665594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57547918-T-C

http://identifiers.org/hco/3/GRCh38#99666140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57547540-A-C

99666667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57546990-G-A

99666777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57546903-C-T

http://identifiers.org/hco/3/GRCh38#99667110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57546612-C-A

99667174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57546551-C-T

99667217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57546503-T-A

99667217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57546503-T-C

99667782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57545968-G-A

http://identifiers.org/hco/3/GRCh38#99668074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57545682-A-C

99668315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57545432-C-T

99668547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57545223-A-G

99668652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57545109-C-G

99668785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544974-C-T

99668870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544889-A-G

99668889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544869-T-G

99669198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544641-T-G

99671406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544006-A-G

http://identifiers.org/hco/3/GRCh38#99671416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57543996-A-C

99671471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543923-T-C

99671911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543505-T-A

99671965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543455-C-T

99671970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543450-G-T

99672120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543290-T-C

99672646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57542952-T-A

99672711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57542893-T-G

99672803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57542739-C-T

99672879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57542611-C-T

99673090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57542399-G-A

http://identifiers.org/hco/3/GRCh38#99673118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57542371-A-C

99673354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57540777-T-G

99673561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57540572-C-T

99673694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57540414-A-T

99673945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57540199-T-C

99674110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57540020-T-G

99674153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539976-A-G

99674170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539960-A-G

http://identifiers.org/hco/3/GRCh38#99674546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57539607-C-A

99674679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539475-A-T

99674732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539409-T-C

99675031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539126-T-A

99675157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57538990-A-G

http://identifiers.org/hco/3/GRCh38#99675211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57538936-A-C

99675231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57538916-T-G

99675248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57538893-C-T

99675279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57538849-T-C

http://identifiers.org/hco/3/GRCh38#99675386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57538738-C-A

99675386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57538738-C-G

99675463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57538641-T-A

99675678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57538158-A-G

99675720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57538116-A-T

99675851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57537986-G-T

99675954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57537885-T-C

http://identifiers.org/hco/3/GRCh38#99676267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57537585-A-C

99676858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57537084-A-T

99676920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57537012-T-A

99677310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57536555-T-C

99677402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57536478-C-T

99677478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57536409-G-A

99677571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57536317-G-A

99677690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57536199-A-G

http://identifiers.org/hco/3/GRCh38#99677724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57536165-C-A

99677724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57536165-C-T

99677898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57535991-T-C

99677937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57535949-G-T

99678178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57535705-T-A

http://identifiers.org/hco/3/GRCh38#99678566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57535332-C-A

99678569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57535329-T-A

99678569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57535329-T-C

99678602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57535295-T-C

99678973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534824-A-G

99679119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534662-C-G

99679190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534598-C-T

99679261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534527-T-C

99679282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534505-G-T

99679616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534231-G-A

99679616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534231-G-T

99679747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534129-A-G

99679779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57534096-T-A

99679929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57533940-T-G

99681449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533713-A-T

99681561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533581-G-A

http://identifiers.org/hco/3/GRCh38#99681732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57533405-C-A

http://identifiers.org/hco/3/GRCh38#99682083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57533063-C-A

99682083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533063-C-T

99682642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533000-G-A

99682668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57532974-A-G

http://identifiers.org/hco/3/GRCh38#99682794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57532870-A-C

99682794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57532870-A-G

99682837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57532828-A-T

99683395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57532380-G-A

99683395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57532380-G-C

99690459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57530083-T-C

http://identifiers.org/hco/3/GRCh38#99690867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57529688-C-A

99690870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57529685-G-C

99691420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57529321-T-A

http://identifiers.org/hco/3/GRCh38#99691441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57529297-C-A

99691466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57529275-G-A

99691505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57529236-T-C

99691506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57529235-T-C

99691559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57529174-A-G

99691612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57529122-A-G

99691627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57529110-T-C

99691804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57528962-A-G

99691941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57528840-T-C

99692063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57528713-G-T

99692112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57528671-T-G

http://identifiers.org/hco/3/GRCh38#99695675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57527130-C-A

99695726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57527058-T-C

99695775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57527012-C-T

99696245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57526857-T-C

99696425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57526688-G-A

99696535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57526597-G-C

http://identifiers.org/hco/3/GRCh38#99697384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57526074-A-C

99697455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57526023-A-G

99697524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57525953-A-T

99705605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524998-A-G

99705683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524919-A-G

99705730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524872-G-A

99705753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524849-T-C

99705820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524798-A-G

99706027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524598-A-G

99706367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57524185-T-G

99706973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57523696-T-C

99706976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57523692-T-C

http://identifiers.org/hco/3/GRCh38#99706978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57523690-C-A

99706980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57523688-G-A

99706990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57523678-G-T

99707004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57523650-T-C

99707284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57523145-T-C

99708043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57522587-T-C

99709509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57520883-A-T

99710104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57519516-G-C

99710221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57519347-G-A

99710502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57519065-A-G

99710660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57518903-G-A

99711090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57518466-T-C

http://identifiers.org/hco/3/GRCh38#99711346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57518180-C-A

99711856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57517624-T-G

99711912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57517567-G-A

99712135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57517347-T-C

99712460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57517024-C-T

http://identifiers.org/hco/3/GRCh38#99712593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57516435-C-A

99713132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57515667-G-T

99713191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57515611-A-T

99714027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57514821-T-C

99714719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57514137-G-A

99714719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57514137-G-C

99714757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57514099-A-G

99714758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57514098-G-A

99714758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57514098-G-C

99714882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57513709-T-C

99714882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57513709-T-G

99715322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57513309-A-G

99715833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57512811-G-A

99716547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57511398-T-C

99716684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57511273-T-G

99716949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57511005-T-C

99717160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57510807-T-C

99717160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57510807-T-G

99719909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57510429-T-C

99720093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57510235-T-C

99720299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57509345-A-G

99720471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57509208-T-C

99720479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57509200-T-C

99720536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57509156-C-T

99720691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57508998-G-A

99720734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57508955-A-G

99721033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57508688-G-A

99722657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507900-C-T

http://identifiers.org/hco/3/GRCh38#99722710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57507846-C-A

99722803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507754-A-G

http://identifiers.org/hco/3/GRCh38#99722862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57507702-C-A

99722862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507702-C-T

99722866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507697-G-A

99722866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507697-G-T

99723549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507032-T-C

99723704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57506869-G-A

http://identifiers.org/hco/3/GRCh38#99723954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57506650-C-A

99723954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57506650-C-T

99724438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57506148-G-C

99724461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57506123-C-T

http://identifiers.org/hco/3/GRCh38#99724499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57506086-C-A

99724664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57505930-A-T

99724768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57505830-C-T

99728479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504871-G-A

99728572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504837-T-A

99728835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504627-A-T

99729248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504237-C-T

99729330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57504156-A-T

99729624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503893-T-C

http://identifiers.org/hco/3/GRCh38#99729681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57503840-A-C

99729789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503785-G-A

99729893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503684-G-A

99730383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503218-A-T

99730425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503178-G-T

99730507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57503036-T-C

99730632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502885-G-A

http://identifiers.org/hco/3/GRCh38#99731013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57502491-A-C

99731023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502481-A-G

99731162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502140-A-G

99731184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502118-T-G

99731290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57502014-G-A

99742295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500893-G-A

99742389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500804-A-G

99744539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500124-A-T

99744573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500090-C-T

99744643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57500025-A-G

99744688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57499980-A-G

99744717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57499960-A-G

99744717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57499960-A-T

99744900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57498813-C-T

99745057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57498647-T-C

99746170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57497424-T-G

http://identifiers.org/hco/3/GRCh38#99746425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57497186-C-A

99746439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57497172-T-C

99746448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57497163-C-G

99746463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57497148-T-C

99746465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57497146-G-A

99746721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496890-C-T

99747059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496556-G-T

99747191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496440-A-T

99747242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496390-T-C

99747317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496315-A-G

http://identifiers.org/hco/3/GRCh38#99747318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57496314-C-A

99747318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496314-C-T

99747626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57496012-G-A

99747643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495995-G-A

99747687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495951-A-G

http://identifiers.org/hco/3/GRCh38#99748066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57495588-C-A

99748066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495588-C-T

99748150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495502-C-G

99748370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495282-A-G

99748447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495233-G-A

99748447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495233-G-T

99748590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57495090-G-C

99748808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57494876-A-G

99749422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57494196-C-G

99749654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57493836-T-C

99750610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57493127-T-C

99750972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57492771-A-G

99751639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57492414-A-T

99751965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57492081-A-G

99752144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57491163-C-G

99752144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57491163-C-T

99753190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57490238-C-T

99753292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57490143-G-A

99753292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57490143-G-C

99753352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57490069-A-G

99753437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57489986-G-C

99753545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, undefined
orthologous variants: 57489881-T-C

http://identifiers.org/hco/3/GRCh38#99753570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#57489858-A-C

99753832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57489591-T-C

99754367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57488487-G-A

http://identifiers.org/hco/3/GRCh38#99754892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57487445-C-A

99756731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57487165-A-G

99756738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57487158-G-T

99756794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57487094-T-C

99756914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57486959-G-T

99757374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57486505-G-A

99757402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57486476-T-C

99758097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485843-T-C

99758479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485460-G-T

99758498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485441-A-T

99758533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485406-A-G

99758669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485277-G-A

99758880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485085-T-C

99758906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57485059-T-A

99759028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57484965-C-T

99759682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57484358-T-C

99759692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57484347-T-G

99759693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57484346-G-A

99759823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57484218-A-T

99759850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57484191-T-C

99760109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57483904-A-G

99760185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57483810-G-T

99760191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57483804-G-A

99760385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57483623-C-T

99760925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57483088-C-T

99761125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57482896-A-G

99761260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57482771-C-T

99761987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57482090-G-A

99762123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57481952-T-C

99762239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57481861-A-G

99763184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57481039-G-A

http://identifiers.org/hco/3/GRCh38#99763216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57481007-C-A

99763741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57480592-C-G

http://identifiers.org/hco/3/GRCh38#99763776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57480561-A-C

99763802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57480533-C-T

99764034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57480468-G-A

99764834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57479531-G-A

99765107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57479100-A-G

99765266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57478967-C-T

99765374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57478817-A-T

99765464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57478725-A-G

99766582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57477666-G-A

99767144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57477418-C-G

99767195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57477368-T-C

99767195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57477368-T-G

99767570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57476970-G-A

99767763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57476781-T-C

99767856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57476685-T-G

99768159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57476373-G-A

http://identifiers.org/hco/3/GRCh38#99768440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57476115-C-A

99768446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57476109-G-A

99769491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57474437-A-G

99770499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57473482-A-G

99770672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57473299-C-T

99771177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57472852-G-C

99773637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57471596-G-A

99773769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57471470-G-C

99774937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57470149-T-C

99775371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57469692-G-A

99775371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57469692-G-T

99775475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57469587-A-G

http://identifiers.org/hco/3/GRCh38#99775486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57469576-A-C

99775674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57469368-C-T

99775717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57469325-T-C

99776069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57469118-A-T

99776346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468856-T-A

99776399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468804-T-A

99776418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468785-T-C

99776444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468773-G-A

99777387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468345-G-A

99777441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468309-C-G

99777471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468284-C-G

99777506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57468249-T-C

99777774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57467933-C-T

99778180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57467528-C-T

http://identifiers.org/hco/3/GRCh38#99778524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57467272-A-C

99778628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57467176-G-A

99778738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57467066-A-G

99778763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57467041-G-A

99778763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57467041-G-C

99778959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57466825-G-A

99779059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57466731-G-C

99779137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57466653-G-A

99779404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57466367-G-T

99780660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57464752-T-C

99781223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57464192-T-C

99781223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57464192-T-G

99781372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57464049-C-T

99782145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57462599-G-A

99782195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57462551-T-C

99782207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57462539-T-C

99783021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57462088-G-A

99783036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57462073-G-A

99783036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57462073-G-T

99783129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57461980-G-C

99783445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57461699-T-C

http://identifiers.org/hco/3/GRCh38#99783447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57461697-A-C

99785383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57459140-C-T

99785457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57459058-G-C

99785457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57459058-G-T

99785564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458972-G-T

99785628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458903-G-A

99785784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458809-C-T

http://identifiers.org/hco/3/GRCh38#99785852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57458762-A-C

99785909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458698-A-G

99785993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458620-A-T

99785995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458617-G-A

99786098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458518-C-T

99786103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57458513-G-A

99786600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57457800-C-T

99786648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57457751-A-G

99786829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57457572-G-C

99787094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57457414-A-T

99787446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57457102-A-G

http://identifiers.org/hco/3/GRCh38#99787553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57457017-C-A

99787553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57457017-C-T

99787596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57456974-T-C

99787981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57456631-C-T

99788078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57456549-T-C

99788374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57456233-T-A

99788439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57456169-G-A

99788715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57455882-A-G

99789039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57455400-T-C

99789081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57455186-A-G

99789474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57454799-T-C

99789608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57454670-C-T

99789684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57454594-T-A

99790500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453693-C-T

99790597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453086-T-C

99790624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453055-C-T

http://identifiers.org/hco/3/GRCh38#99790637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57453042-C-A

99790637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453042-C-G

99790637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453042-C-T

99790640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453039-G-A

99790640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57453039-G-T

99791117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57452558-T-C

http://identifiers.org/hco/3/GRCh38#99791137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57452538-C-A

99791267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57452161-T-G

99791425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57451998-C-T

99791443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57451984-A-T

99791767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57451667-G-A

99791859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57451582-T-C

99791878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57451573-A-G

99792171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57451011-G-A

99792302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57450886-G-A

99792378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57450811-A-G

http://identifiers.org/hco/3/GRCh38#99792450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57450746-C-A

99792899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57450316-G-C

99793157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57450022-A-G

99793576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57449494-A-T

99793611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57449460-T-A

99794071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57449308-G-T

99794104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57449275-T-A

99794105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: intron variant
orthologous variants: 57449274-A-G

99794529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57448876-C-T

99794601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: stop gained
orthologous variants: 57448804-C-T

http://identifiers.org/hco/3/GRCh38#99794784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57448621-C-A

99794784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57448621-C-T

99795177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57448228-G-T

99795264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57448141-C-T

http://identifiers.org/hco/3/GRCh38#99795390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57448015-C-A

99795390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57448015-C-T

99795408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57447997-G-A

99795408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57447997-G-T

http://identifiers.org/hco/3/GRCh38#99795522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57447883-C-A

99795522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57447883-C-T

99795693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57447715-C-T

99795771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: missense variant
orthologous variants: 57447637-G-A

99796077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: synonymous variant
orthologous variants: 57447331-C-T

99796548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57446874-A-G

http://identifiers.org/hco/3/GRCh38#99796553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57446869-A-C

99796889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57446541-G-A

99796889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57446541-G-T

99797740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57446015-G-A

99797788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57445968-G-A

http://identifiers.org/hco/3/GRCh38#99797938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57445838-C-A

99797945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57445831-G-T

http://identifiers.org/hco/3/GRCh38#99798296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#57445487-A-C

99798386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57445397-T-C

99798403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57445381-T-C

99798562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57445237-A-G

99798963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57444872-C-T

99799017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57444819-C-T

99799112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2215
most severe consequence: 3 prime UTR variant
orthologous variants: 57444725-T-C