27321898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56648004-G-A

27321898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56648004-G-C

27321992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56647909-G-T

27322748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56647190-C-T

27322903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56647071-G-A

27322931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56647036-G-A

27322947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56647020-C-T

27325627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56636297-G-A

27325653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56636271-G-A

27326030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635954-G-A

27326188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635774-C-T

27326244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635695-G-A

27326534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635322-T-C

27326623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635233-C-G

27326623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635233-C-T

http://identifiers.org/hco/15/GRCh38#27326664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56635196-C-A

27326664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635196-C-T

27326716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635142-A-G

27326716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635142-A-T

27326747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635110-A-G

27326765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56635069-T-C

27328373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56633432-A-G

27328418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56633390-G-A

27328528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56633274-G-T

27328849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 56632410-C-G

27328849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 56632410-C-T

27328858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: missense variant
orthologous variants: 56632401-G-A

27328858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: missense variant
orthologous variants: 56632401-G-C

27328894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56632365-T-C

27328916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56632338-G-A

27329034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56632234-G-A

27329034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56632234-G-T

27329779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56631873-A-G

http://identifiers.org/hco/15/GRCh38#27330874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56630155-A-C

27330874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56630155-A-G

27338603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56622940-A-G

27338603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56622940-A-T

27340461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56621052-A-T

27340544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56620967-T-C

http://identifiers.org/hco/15/GRCh38#27340576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56620938-C-A

http://identifiers.org/hco/15/GRCh38#27340688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56620819-C-A

27340688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56620819-C-T

27340716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56620802-A-G

27340810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620722-A-G

27340813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620719-A-G

27340913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620662-T-G

27341023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620585-A-G

27341059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620546-A-G

27341066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620536-G-T

http://identifiers.org/hco/15/GRCh38#27341077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56620525-C-A

27341077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620525-C-T

27341145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620466-T-G

27341334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56620247-G-A

http://identifiers.org/hco/15/GRCh38#27341402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56620197-A-C

27341628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619981-C-T

http://identifiers.org/hco/15/GRCh38#27341886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56619739-C-A

27341902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619723-C-T

27342104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619551-C-T

27342437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619198-C-T

27342557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619091-G-A

27342585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619063-G-A

27342585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56619063-G-C

27342899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56618757-A-G

27343086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56612053-C-T

27343134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, undefined
orthologous variants: 56612014-G-A

27343134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, undefined
orthologous variants: 56612014-G-C

27343395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56611706-A-G

27343774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56611325-T-A

27343814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56611273-A-G

27343989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56611083-C-T

http://identifiers.org/hco/15/GRCh38#27343991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56611081-C-A

27344485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56610521-G-A

27357620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56600414-T-G

27357760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56600289-G-T

27357866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56600212-C-T

27357867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56600211-T-C

27358014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56600052-A-G

27358302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56599477-C-T

27358339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56599401-A-G

27358432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56599323-C-T

27358763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56597122-G-T

27359595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56591801-A-G

27359703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56591680-A-G

27359703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56591680-A-T

27359898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56591462-C-T

http://identifiers.org/hco/15/GRCh38#27361657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56569473-A-C

27361677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56569454-G-A

27361717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56569419-G-A

27362047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56569102-C-T

http://identifiers.org/hco/15/GRCh38#27362154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56569013-C-A

27362154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56569013-C-T

27362690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56568489-C-T

http://identifiers.org/hco/15/GRCh38#27362711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56568443-C-A

27362711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56568443-C-T

27362863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56568253-T-C

27362908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56568215-G-T

27363028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56568090-A-G

27363150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567979-G-A

27363183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567946-C-T

27363223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567905-A-G

27363254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567862-G-A

27363254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567862-G-T

27363274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567842-T-C

27363302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567814-A-G

27363306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567810-G-T

27363344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56567772-T-C

http://identifiers.org/hco/15/GRCh38#27364340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56564839-C-A

27364340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56564839-C-T

27364350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56564828-A-G

27364464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56564708-G-T

27364509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56564665-G-A

27364509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56564665-G-C

27364698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56564502-G-A

27367792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56561964-T-C

27370380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56554160-G-A

27370432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56554119-A-G

27370456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56554097-T-C

27370457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56554096-G-C

27370504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56554049-G-A

27370530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56554016-C-T

http://identifiers.org/hco/15/GRCh38#27370709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56553858-A-C

27371038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56553525-T-G

27371212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56553369-A-G

27371281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56553301-A-T

27371282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56553300-T-C

27371647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56552942-A-G

27371780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56552852-T-C

27372061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56551666-A-G

http://identifiers.org/hco/15/GRCh38#27372205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56551541-A-C

27372269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56551483-T-G

27373673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56549993-A-T

27373695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56549971-G-C

http://identifiers.org/hco/15/GRCh38#27373909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56549761-A-C

27373909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56549761-A-G

27378580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56548800-C-G

27378580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56548800-C-T

27378857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56548583-A-G

27378933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56548523-T-A

27379028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56548226-G-A

27379115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56548042-T-G

27379307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56547871-C-T

27379330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56547848-T-C

27379722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56547432-C-T

27380013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56547197-C-T

27381750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56546658-T-C

27381775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56546633-T-C

27381900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56546487-G-C

27381941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56546447-C-T

27382603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56545847-T-C

27382739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56545732-T-C

27382824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56545658-C-T

27383150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56545315-C-T

27389530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56537493-T-G

27389682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56537330-G-A

http://identifiers.org/hco/15/GRCh38#27389868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56537149-C-A

27389868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56537149-C-T

27389912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56537105-G-A

27390172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56536846-T-C

27390219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56536806-C-T

27390247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56536778-C-T

27397418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56528006-A-G

27397418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56528006-A-T

27397661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56527830-C-G

27397720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56527768-C-T

27397757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56527730-A-G

27399218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56525315-C-G

27399360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, undefined
orthologous variants: 56525181-G-A

27399423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56525138-G-A

27399423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56525138-G-C

27399423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56525138-G-T

27399522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56525047-C-T

27399616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56524965-C-G

http://identifiers.org/hco/15/GRCh38#27399819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56524796-C-A

27399828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56524789-A-G

27399846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56524772-A-G

27399929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56524692-G-A

27399929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56524692-G-T

27400031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56524608-A-G

27400332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56522617-C-T

27400692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56522261-G-C

27400718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56522233-G-C

27400718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56522233-G-T

http://identifiers.org/hco/15/GRCh38#27401876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56517374-C-A

27402093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56517197-T-A

27413542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56495483-T-G

http://identifiers.org/hco/15/GRCh38#27413983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56495023-A-C

27414266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56494761-T-A

27414515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56494550-T-A

http://identifiers.org/hco/15/GRCh38#27414678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56494418-C-A

27414681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56494415-G-A

27414698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56494404-C-G

27414698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56494404-C-T

27418689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56493228-C-T

http://identifiers.org/hco/15/GRCh38#27418748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56493197-C-A

27418941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56493031-C-T

27418942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56493030-T-C

http://identifiers.org/hco/15/GRCh38#27418987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56492985-C-A

27418987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56492985-C-T

http://identifiers.org/hco/15/GRCh38#27418994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56492979-C-A

27419036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56492939-G-A

27419037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56492938-G-T

27419136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492848-A-G

27419139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492845-G-A

27419139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492845-G-T

27419162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492822-T-C

http://identifiers.org/hco/15/GRCh38#27419259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56492740-C-A

27419273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492726-T-C

27419294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492697-T-A

27419323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492656-T-C

http://identifiers.org/hco/15/GRCh38#27419349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56492632-A-C

27419360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492620-A-G

27419360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492620-A-T

27419905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56492123-T-G

27434418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56469162-G-A

27434465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56469208-G-A

http://identifiers.org/hco/15/GRCh38#27434506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56469249-C-A

27439907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474223-C-T

27439979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474305-G-A

27440080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474402-T-A

27440141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474449-C-G

27440166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474475-C-G

27440168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474477-T-G

27440335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56474636-C-T

http://identifiers.org/hco/15/GRCh38#27440583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56474865-C-A

http://identifiers.org/hco/15/GRCh38#27440811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56475064-C-A

27441251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475480-T-C

27441272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475491-A-G

27441340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475536-G-A

27441536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475712-A-G

27441550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475726-C-G

27441551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475727-C-T

http://identifiers.org/hco/15/GRCh38#27441751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56475896-C-A

27441768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475913-G-A

27441772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475917-T-C

27441772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475917-T-G

27441838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56475977-C-T

27442019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56476187-C-G

27442039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56476206-A-G

http://identifiers.org/hco/15/GRCh38#27442096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56476274-C-A

27442339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56476452-C-T

http://identifiers.org/hco/15/GRCh38#27448862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56460195-A-C

27448887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56460174-T-C

27449016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56460047-A-T

27449095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56459988-T-A

27449423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56459684-T-C

27449634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56459469-T-G

27449668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56459437-T-C

27449929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56459249-T-C

27449973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56459202-A-G

27450287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56458934-C-T

27450288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56458933-G-A

27457843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56452038-G-C

27457927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56451972-C-T

27458149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56451766-T-C

27458343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56451622-A-G

27458419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56451547-C-T

27458617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56451370-G-A

27474272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56426672-A-T

27474337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56426080-A-G

27474408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56426011-C-G

27474436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425990-G-A

27474525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425937-C-G

27474525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425937-C-T

http://identifiers.org/hco/15/GRCh38#27474550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56425909-C-A

27474550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425909-C-T

27474592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425863-C-T

27474696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425764-A-G

27474701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425759-A-G

27474737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56425719-T-C

http://identifiers.org/hco/15/GRCh38#27474790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56425661-C-A

http://identifiers.org/hco/15/GRCh38#27480517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56423226-A-C

http://identifiers.org/hco/15/GRCh38#27480518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56423225-A-C

27480518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56423225-A-G

27480518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56423225-A-T

27480536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56423220-G-A

27480536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56423220-G-T

27480540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56423216-T-C

27480954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56422797-G-T

http://identifiers.org/hco/15/GRCh38#27481081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56422643-C-A

27481081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56422643-C-T

http://identifiers.org/hco/15/GRCh38#27481258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56422518-C-A

27481404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56422391-T-A

27481531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56422276-A-G

http://identifiers.org/hco/15/GRCh38#27481600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56422202-C-A

27481777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron variant
orthologous variants: 56422059-T-C

27485869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418428-G-C

27486017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418302-A-G

27486166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56418150-C-T

27486449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417878-T-C

27486567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56417773-G-A

27486925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416541-G-A

27486984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416482-T-C

27487081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416399-A-G

27487106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416374-T-C

http://identifiers.org/hco/15/GRCh38#27487292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56416193-C-A

27487412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56416080-C-T

27487573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415923-C-T

27492060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415613-A-G

27492493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415223-A-G

27492529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56415187-C-T

http://identifiers.org/hco/15/GRCh38#27493191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56414209-C-A

27493191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414209-C-T

27493233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414164-T-C

27493292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414114-A-G

27493308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414097-G-A

27493356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56414042-A-G

27493762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413719-G-A

27493898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413597-G-T

27493992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413517-G-A

27493992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413517-G-C

27494070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413434-G-A

27494094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413416-C-T

27494208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413295-C-G

27494261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413239-A-G

27494261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413239-A-T

27494350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56413178-G-A

27497711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406901-G-A

27497748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406865-C-T

27497942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406702-C-T

27498169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406494-C-G

27498169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406494-C-T

27498289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56406363-T-C

27499086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405815-G-A

27499174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56405731-A-G

http://identifiers.org/hco/15/GRCh38#27499502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56405436-C-A

http://identifiers.org/hco/15/GRCh38#27500894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56403652-A-C

27500894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403652-A-T

27500914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403630-C-T

27501282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403587-G-A

27501309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403560-T-C

27501353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403524-A-G

27501438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403442-T-C

27501438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403442-T-G

27501534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403349-G-T

27501571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403313-A-T

27501832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403021-G-A

27501832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56403021-G-C

27501942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402925-T-C

27502008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56402863-A-G

27510936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56387324-A-G

27519581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56385221-C-T

27519594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56385208-G-T

27519645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56385157-T-A

27519847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384969-T-C

27519847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384969-T-G

27519966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56384851-T-C

27520028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56384789-A-G

27520131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56384686-T-G

http://identifiers.org/hco/15/GRCh38#27520138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56384679-A-C

27520197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384620-A-G

27520217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384602-G-A

27520224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56384595-A-G

27527361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379604-A-G

27527362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379603-T-C

http://identifiers.org/hco/15/GRCh38#27527397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56379569-C-A

27527397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379569-C-G

27527411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379555-A-T

27527480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56379486-A-G

27527483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56379483-T-C

27527556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56379410-C-T

http://identifiers.org/hco/15/GRCh38#27527608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56379358-C-A

27527624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56379342-A-G

27527643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379320-G-A

27527667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379296-G-A

http://identifiers.org/hco/15/GRCh38#27527701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56379262-C-A

27527785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379206-G-T

27527846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379146-T-A

27527846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379146-T-G

27527849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56379143-T-C

http://identifiers.org/hco/15/GRCh38#27528096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56378934-A-C

27528096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378934-A-G

27528215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378813-G-A

27528874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378617-T-C

27528874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378617-T-G

27528937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378551-T-C

27529098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378477-A-G

27529098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378477-A-T

27529362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378306-T-C

27529435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378257-A-G

27529559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378180-C-T

27529657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56378083-G-A

http://identifiers.org/hco/15/GRCh38#27529719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56378045-A-C

27529748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377975-A-T

http://identifiers.org/hco/15/GRCh38#27529881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56377841-C-A

http://identifiers.org/hco/15/GRCh38#27529981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56377764-C-A

http://identifiers.org/hco/15/GRCh38#27530028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56377738-A-C

27530146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377603-A-G

27530196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377566-C-G

27530242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377521-C-T

27530301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377465-C-T

27530311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377455-G-A

27530315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377451-G-A

27530490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56377279-T-C

27530623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56377155-T-C

27530661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56377124-A-T

27530682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 56377103-C-T

27530704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56377082-C-G

27530705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56377081-C-T

27530824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376961-A-T

27530830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376955-C-T

27530846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376939-T-C

http://identifiers.org/hco/15/GRCh38#27530861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56376924-A-C

27530870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376915-G-A

27530870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376915-G-T

27530872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376913-G-A

27530872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376913-G-T

27530892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376892-T-A

27530892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376892-T-C

27530892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56376892-T-G

http://identifiers.org/hco/15/GRCh38#27530918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56376865-C-A

http://identifiers.org/hco/15/GRCh38#27530921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56376862-C-A

27530921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376862-C-T

27530928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56376855-T-G

27531658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56375208-C-T

27532005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374869-A-G

27532045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374829-C-T

http://identifiers.org/hco/15/GRCh38#27532050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56374824-C-A

27532050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374824-C-T

27532466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374567-T-A

27532466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374567-T-C

27532466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374567-T-G

27532467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374566-G-T

http://identifiers.org/hco/15/GRCh38#27532486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56374548-C-A

27532486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56374548-C-T

27532777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 56374263-A-G

27532953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56374087-G-A

27532961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56374075-G-A

27532976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56374060-G-T

http://identifiers.org/hco/15/GRCh38#27532979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56374057-C-A

27532979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56374057-C-T

27532993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56374042-T-C

27533091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373916-T-C

27533126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373879-G-A

27533197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373817-A-T

27533228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373787-G-C

27533229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373786-A-G

27533229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373786-A-T

27533232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373783-C-T

http://identifiers.org/hco/15/GRCh38#27533254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56373762-C-A

27533254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373762-C-T

http://identifiers.org/hco/15/GRCh38#27533356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56373673-C-A

27533356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373673-C-T

27533376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373653-G-T

http://identifiers.org/hco/15/GRCh38#27533425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56373613-A-C

27533425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373613-A-G

27533428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373610-A-G

27533437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373601-T-C

27533581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373463-G-T

http://identifiers.org/hco/15/GRCh38#27533614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56373430-C-A

27533614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373430-C-T

http://identifiers.org/hco/15/GRCh38#27533684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56373354-C-A

27533817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373273-A-T

27533857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56373247-A-G

http://identifiers.org/hco/15/GRCh38#27534530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56372850-C-A

27534644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372742-G-T

27534701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372689-G-T

27534937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372446-T-C

27535048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372335-T-A

27535048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372335-T-G

27535049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372334-G-C

27535071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372320-C-T

27535157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372274-C-T

27535301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56372132-T-G

http://identifiers.org/hco/15/GRCh38#27535641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56372004-C-A

27535712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56371942-A-G

27535859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56371810-A-G

27535979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56371694-G-T

27535993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56371680-G-A

27535993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56371680-G-C

27535993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56371680-G-T

http://identifiers.org/hco/15/GRCh38#27536597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56371140-C-A

http://identifiers.org/hco/15/GRCh38#27536649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56371101-C-A

27536801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370973-A-G

27536948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56370826-T-C

27536976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56370798-C-T

27537001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56370774-C-T

27537049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56370727-C-G

27537063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 56370713-T-A

27537128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 56370662-A-T

27537191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370611-C-G

27537191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370611-C-T

http://identifiers.org/hco/15/GRCh38#27537270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56370542-C-A

27537286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370526-A-G

27537513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370373-C-G

27537513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370373-C-T

27537583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370315-C-T

27537711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56370189-T-C

http://identifiers.org/hco/15/GRCh38#27538028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56370066-A-C

27538649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56369597-A-G

http://identifiers.org/hco/15/GRCh38#27538686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56369559-C-A

27539071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368860-C-T

http://identifiers.org/hco/15/GRCh38#27539171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56368766-C-A

http://identifiers.org/hco/15/GRCh38#27539201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56368738-C-A

27539243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368701-G-A

27539262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368674-G-T

27539347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368589-G-T

27539724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368271-A-G

27539731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368264-G-T

27539913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368091-A-G

27539973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56368050-C-T

27540406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367660-A-T

27540425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367641-T-C

27540699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367417-G-A

27540771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367351-G-T

27540787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367336-G-A

27540787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367336-G-T

http://identifiers.org/hco/15/GRCh38#27540849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56367274-C-A

27540849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367274-C-T

27540853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 56367270-C-T

27541421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56366749-G-T

http://identifiers.org/hco/15/GRCh38#27541429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56366741-C-A

http://identifiers.org/hco/15/GRCh38#27541434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56366736-C-A

27541434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56366736-C-T

27541445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56366725-G-A

27541445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56366725-G-T

27541826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56366392-G-A

http://identifiers.org/hco/15/GRCh38#27541892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56366326-A-C

27541892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 56366326-A-G

http://identifiers.org/hco/15/GRCh38#27541917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4088
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#56366278-C-A