186046366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200105-C-T

186046394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200133-G-T

http://identifiers.org/hco/3/GRCh38#186046509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22200211-C-A

186046509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200211-C-G

186046561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200259-G-A

186046561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200259-G-T

http://identifiers.org/hco/3/GRCh38#186046627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22200320-C-A

186046639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200332-G-A

186046639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200332-G-T

186046646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200339-T-C

186046646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200339-T-G

http://identifiers.org/hco/3/GRCh38#186047085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22200717-C-A

186047089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200721-T-A

186047144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200760-T-C

186047157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200770-G-A

186047171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200784-A-G

186047192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200812-A-G

186047228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200848-T-G

186047287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200914-A-G

186047324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22200952-G-T

186047536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201178-G-A

186047558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201200-A-G

http://identifiers.org/hco/3/GRCh38#186047585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22201227-C-A

186047585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201227-C-T

http://identifiers.org/hco/3/GRCh38#186047686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22201316-C-A

186047743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201373-G-A

186047744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201374-G-T

http://identifiers.org/hco/3/GRCh38#186047957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22201581-C-A

http://identifiers.org/hco/3/GRCh38#186047959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22201583-C-A

186047962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201586-A-G

186048037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201661-C-T

186048125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201739-C-T

186048140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201754-T-G

186048206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201807-T-C

186048236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22201840-G-T

186048577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3 prime UTR variant
orthologous variants: 22202158-C-T

186048590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22202171-G-A

186048601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22202182-G-T

186048627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22202208-C-T

186048679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22202260-C-T

186048733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22202314-G-A

186048733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22202314-G-T

186048843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22202424-G-A

186048881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22202462-T-C

http://identifiers.org/hco/3/GRCh38#186048884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22202465-A-C

186048906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22202490-T-A

186048906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22202490-T-C

186049060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22202665-A-G

186049084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22202690-C-T

186051489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22204598-A-G

186051529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22204641-C-T

186051694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22204810-T-C

http://identifiers.org/hco/3/GRCh38#186051892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22205303-A-C

186051892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205303-A-G

http://identifiers.org/hco/3/GRCh38#186051909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22205390-C-A

186051909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205390-C-T

186051923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205404-G-A

186051923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205404-G-T

186051933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205414-T-C

186051938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205419-C-T

http://identifiers.org/hco/3/GRCh38#186051964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22205445-C-A

186051964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205445-C-T

186051988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205469-A-G

http://identifiers.org/hco/3/GRCh38#186051994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22205474-A-C

186052123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22205600-C-T

186052173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205646-C-T

http://identifiers.org/hco/3/GRCh38#186052227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22205669-C-A

186052238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205680-G-T

186052260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205702-G-A

186052260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205702-G-T

186052449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205883-A-G

186052546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22205980-T-G

186052631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22206065-T-C

186052631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22206065-T-G

186053339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22206750-T-A

186053398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22206806-G-A

186053829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22207809-G-A

186054108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208041-T-C

186054149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208080-C-T

186054288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208201-T-C

186054352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208279-A-G

186054451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208385-C-T

186054512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208449-G-A

186054832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22208773-C-T

186054979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22209073-C-T

186055142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22209238-A-G

186055312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22209417-G-T

186055749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22210061-C-T

186056042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22210263-A-G

186056217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22210441-A-G

http://identifiers.org/hco/3/GRCh38#186056993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22211323-A-C

http://identifiers.org/hco/3/GRCh38#186057009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22211339-C-A

186057009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22211339-C-G

186057009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22211339-C-T

186057019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22211364-A-G

186057019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22211364-A-T

186057048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22211393-C-T

186057141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22211471-T-G

http://identifiers.org/hco/3/GRCh38#186057162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22211492-C-A

186057484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22211798-T-A

186057484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22211798-T-C

186057484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22211798-T-G

186057545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22211859-C-T

http://identifiers.org/hco/3/GRCh38#186057575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22212047-A-C

186057575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22212047-A-G

186057617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22212110-G-A

186057617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22212110-G-T

186057680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22212184-G-C

186057754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22212256-T-C

186058060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22212531-T-C

186059414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22213583-C-G

186059414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22213583-C-T

186059476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22213677-T-C

186059489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22213690-A-G

186059995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22214454-C-G

186059995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22214454-C-T

http://identifiers.org/hco/3/GRCh38#186060013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22214468-C-A

186060013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22214468-C-T

186060684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22215094-G-C

186060785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22215188-G-C

http://identifiers.org/hco/3/GRCh38#186061000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22215410-C-A

http://identifiers.org/hco/3/GRCh38#186061056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22215470-C-A

186061158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22215560-G-T

186061542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22216038-G-C

186061791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22216263-C-G

186063601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217090-A-G

186063880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217367-T-C

http://identifiers.org/hco/3/GRCh38#186064006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22217683-A-C

186064006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217683-A-G

186064031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217708-T-A

186064168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217822-G-A

186064168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217822-G-C

186064168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22217822-G-T

186064255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22217897-T-C

186064334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22217976-G-A

186064515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22218160-G-T

186064531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22218181-C-T

186064532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22218182-A-G

186064578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22218248-T-G

186064579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22218249-G-A

186064579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22218249-G-T

186064592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22218262-G-T

186064910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22218892-T-G

186065215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22219135-G-C

186065916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22220525-T-C

186066123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22220726-A-G

186066134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22220737-G-A

186066134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22220737-G-T

186066136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22220739-A-G

186066139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22220742-G-A

186069328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223466-G-C

186069386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223531-G-A

186069386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223531-G-T

186069408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223553-C-T

186070338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223776-C-T

186070339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223777-G-A

186070352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22223790-C-G

186070532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224003-G-A

186070582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22224038-T-C

186070662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224121-G-C

186070752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224214-G-T

186071022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224414-T-C

186071361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224753-C-T

186071362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224754-G-A

186071589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22224943-G-C

186074943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22226745-C-T

186075315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22227059-G-A

http://identifiers.org/hco/3/GRCh38#186075540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22227224-C-A

186075603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22227279-C-G

186075664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22227356-G-A

186076024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22227484-A-G

186076633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22227733-G-A

186076807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22227856-T-C

186077793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228649-T-G

http://identifiers.org/hco/3/GRCh38#186077821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22228682-C-A

186077893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228740-G-T

http://identifiers.org/hco/3/GRCh38#186077992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22228827-C-A

186077992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 22228827-C-T

http://identifiers.org/hco/3/GRCh38#186077993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22228828-C-A

http://identifiers.org/hco/3/GRCh38#186078008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22228841-C-A

186078008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228841-C-T

186078054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228873-C-G

186078054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228873-C-T

186078055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228874-A-G

186078090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228904-G-A

186078090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228904-G-C

186078102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228916-C-T

186078125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22228939-T-C

http://identifiers.org/hco/3/GRCh38#186078133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22228947-C-A

186078295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229123-G-T

186078308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229136-T-C

http://identifiers.org/hco/3/GRCh38#186078329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229161-C-A

186078329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229161-C-T

http://identifiers.org/hco/3/GRCh38#186078332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229164-C-A

186078344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229176-T-C

186078352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229181-T-C

186078352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229181-T-G

http://identifiers.org/hco/3/GRCh38#186078356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229185-C-A

186078356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229185-C-T

http://identifiers.org/hco/3/GRCh38#186078362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229191-C-A

186078367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229196-G-A

186078406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229226-A-G

186078432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229244-G-A

186078664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229413-G-A

186078822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229579-C-T

http://identifiers.org/hco/3/GRCh38#186078901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229618-C-A

http://identifiers.org/hco/3/GRCh38#186078978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229659-C-A

186078978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229659-C-T

http://identifiers.org/hco/3/GRCh38#186078990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229667-C-A

186078990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229667-C-G

186078990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22229667-C-T

186079157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22229790-T-C

186079204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22229820-G-T

http://identifiers.org/hco/3/GRCh38#186079303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22229912-C-A

186079404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22229998-T-A

186079424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230016-A-T

186079425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230017-T-G

186079435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230027-A-G

186079488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230100-G-A

186079488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230100-G-T

186079491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230103-T-A

http://identifiers.org/hco/3/GRCh38#186079674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22230244-A-C

186079674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230244-A-G

186079674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230244-A-T

186079710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230288-T-C

http://identifiers.org/hco/3/GRCh38#186079725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22230303-C-A

186079725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22230303-C-T

http://identifiers.org/hco/3/GRCh38#186079984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22230550-C-A

186079984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 22230550-C-T

http://identifiers.org/hco/3/GRCh38#186080164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22230729-C-A

186080164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22230729-C-T

186080200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22230765-G-T

186080224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22230789-A-T

186080379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22230941-T-C

186080399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22230974-A-G

186080399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22230974-A-T

http://identifiers.org/hco/3/GRCh38#186080476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22231044-C-A

186080476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231044-C-T

186080485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231053-G-A

186080485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231053-G-C

186080485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231053-G-T

186080500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231069-G-C

186080500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231069-G-T

186080652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22231204-T-C

186080767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22231322-A-G

186080799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22231355-A-G

186080839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22231384-C-G

http://identifiers.org/hco/3/GRCh38#186080898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22231448-C-A

186080898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22231448-C-T

186080948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231493-T-G

186081032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231564-T-A

186081032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231564-T-C

186081036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231568-G-A

186081372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22231950-A-G

186081432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22232007-G-C

186081469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22232042-C-T

http://identifiers.org/hco/3/GRCh38#186081771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22232689-C-A

186081775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22232693-C-T

186081877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22232773-G-T

186081956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22233356-T-G

186082225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22233624-T-C

186082327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22233715-C-T

186083200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22234347-C-T

http://identifiers.org/hco/3/GRCh38#186083352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22234494-A-C

186083724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22234875-G-T

186083835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22234972-G-A

186083835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22234972-G-T

186084068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235121-T-C

186084069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235122-G-A

186084073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235126-T-C

186084073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235126-T-G

186084081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235134-T-C

186084111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235150-G-T

186084162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22235187-T-C

186084176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 22235201-C-G

186084313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235320-T-A

186084323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235330-T-A

186084323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235330-T-G

http://identifiers.org/hco/3/GRCh38#186084336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22235340-C-A

186084336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235340-C-T

186084377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235375-G-A

186084384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235382-C-T

186084745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235673-G-C

186084745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235673-G-T

186084753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235681-G-A

186084809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22235734-C-T

http://identifiers.org/hco/3/GRCh38#186084985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22236125-C-A

186085774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22236785-T-C

186086049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22236985-C-T

186086091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237031-C-G

http://identifiers.org/hco/3/GRCh38#186086112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22237044-A-C

186086222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237110-G-A

186086540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237421-T-C

186086590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237482-G-A

186086621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237654-T-C

186086737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237838-G-A

186086768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22237884-G-A

186087129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22238437-G-C

186087129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22238437-G-T

186089036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22238954-T-C

186089069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22238987-A-G

186089480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22239873-C-T

186089520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22239913-T-C

186089798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22240095-T-A

186089829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22240129-A-G

186090015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22240310-T-C

186090128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22240422-T-C

186090141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22240435-T-C

186090567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241156-T-C

http://identifiers.org/hco/3/GRCh38#186090788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22241366-C-A

186090800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241378-G-A

186091339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241441-G-A

186091447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241544-A-G

186091561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241629-A-G

186091575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241647-G-A

186091642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241708-G-A

186091663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241799-A-G

186091784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22241996-T-G

186091921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22242091-C-G

186091979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22242141-G-A

186092100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22242263-T-C

http://identifiers.org/hco/3/GRCh38#186092183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22242341-C-A

186092326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22242470-C-G

186093056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22243010-C-T

http://identifiers.org/hco/3/GRCh38#186093137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22243096-C-A

186093398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22243274-G-A

186093739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22243715-T-G

186093762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22243738-A-G

186095354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245340-A-G

http://identifiers.org/hco/3/GRCh38#186095551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22245577-C-A

186095552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245578-A-G

186095616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245624-C-T

186095634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245649-C-T

186095656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245671-G-T

186095705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245704-T-G

186095820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22245796-C-G

186096549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22246675-A-G

http://identifiers.org/hco/3/GRCh38#186096572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22246698-C-A

186096609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22246727-C-T

186097413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22247339-G-C

186098053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22247948-C-T

186098115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22248012-G-C

186098229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22248115-T-C

http://identifiers.org/hco/3/GRCh38#186098541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22248372-C-A

186099012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22248773-A-G

186099037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22248798-T-C

186099112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22248857-C-G

186099317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22249024-T-C

186099322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22249029-T-C

186099694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22249385-G-C

http://identifiers.org/hco/3/GRCh38#186100225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22249847-C-A

186100998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22250705-T-C

http://identifiers.org/hco/3/GRCh38#186101154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22250872-A-C

186101174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22250896-A-G

186102008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22251836-C-G

186102035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22251863-T-C

186102884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22252226-C-T

186102965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22252308-A-G

186103012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22252352-A-G

186103157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22252507-A-G

186103367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22252748-C-T

186103452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22252857-A-G

186103671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22253047-T-A

186103831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22253170-C-T

186103885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22253225-T-C

186104312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22253630-G-T

http://identifiers.org/hco/3/GRCh38#186105104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22254432-C-A

186105104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22254432-C-T

186105127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22254445-T-A

186105127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22254445-T-C

186105135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22254453-A-G

http://identifiers.org/hco/3/GRCh38#186105195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22254512-C-A

http://identifiers.org/hco/3/GRCh38#186105601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22254929-C-A

186105601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22254929-C-T

186105958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255326-G-T

186105959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255327-G-T

186105978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255346-G-A

186105978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255346-G-C

186105979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255347-G-A

186105989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255351-G-A

186105989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255351-G-T

http://identifiers.org/hco/3/GRCh38#186106042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22255404-C-A

186106042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22255404-C-T

http://identifiers.org/hco/3/GRCh38#186106650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22256130-A-C

186107361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22256807-G-C

186107456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22256904-G-C

186107573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22257037-G-A

186107804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22257282-G-T

186107820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22257298-T-C

http://identifiers.org/hco/3/GRCh38#186108108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22257594-A-C

186108343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22257774-C-T

186108442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22257862-G-A

186108442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22257862-G-T

186108653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22258057-G-C

186108653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22258057-G-T

http://identifiers.org/hco/3/GRCh38#186108672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22258082-C-A

186108676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258091-G-A

186108676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258091-G-T

186108733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258148-G-A

186108733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258148-G-T

http://identifiers.org/hco/3/GRCh38#186108748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22258163-C-A

186108748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258163-C-T

186108778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258193-G-A

186108778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258193-G-T

http://identifiers.org/hco/3/GRCh38#186108779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22258194-C-A

186108779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258194-C-T

http://identifiers.org/hco/3/GRCh38#186108827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22258236-C-A

186108827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 22258236-C-T

http://identifiers.org/hco/3/GRCh38#186108855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22258262-C-A

186108855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22258262-C-T

186108953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22258279-T-A

186108953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22258279-T-C

186108953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22258279-T-G

http://identifiers.org/hco/3/GRCh38#186109132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22258406-C-A

186109132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258406-C-G

186109132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258406-C-T

186109139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258413-T-G

186109149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258416-G-A

186109149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258416-G-T

186109185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258451-T-C

186109715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22258919-A-T

186110163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259344-T-C

186110293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22259471-G-A

186110293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22259471-G-T

186110300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3494
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22259478-T-C