186105958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
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: 2853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22259478-T-C

186110327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259506-G-A

186110327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259506-G-T

http://identifiers.org/hco/3/GRCh38#186110331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22259510-C-A

186110331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259510-C-G

186110331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259510-C-T

186110340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259519-G-A

186110340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259519-G-T

http://identifiers.org/hco/3/GRCh38#186110365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22259527-C-A

186110365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259527-C-T

186110381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259546-C-T

186110384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259549-G-A

186110384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259549-G-T

http://identifiers.org/hco/3/GRCh38#186110385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22259550-C-A

186110385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259550-C-T

186110386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259551-G-T

186110669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22259790-G-A

186110942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22260011-A-G

186110942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22260011-A-T

186110951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22260020-C-T

186111044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22260112-G-A

186112341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22261023-T-C

186112341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22261023-T-G

186112374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22261055-C-T

186113434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22261708-C-T

http://identifiers.org/hco/3/GRCh38#186113544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22261797-A-C

186113554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22261807-A-G

186113986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22262510-G-A

186114055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22262542-G-C

186114118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22262599-A-G

186114128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22262609-T-C

http://identifiers.org/hco/3/GRCh38#186115504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22263867-A-C

186115733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22264113-C-T

186115912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22264282-C-T

186118071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265435-T-G

186118101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265468-G-T

http://identifiers.org/hco/3/GRCh38#186118176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22265533-A-C

186118215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265579-A-G

186118653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265680-G-C

186118710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265737-G-A

186118744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265765-C-T

186118780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265801-T-C

186118946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265957-C-T

186118947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22265958-C-T

186119026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266037-G-A

186119026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266037-G-C

186119102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266113-C-T

http://identifiers.org/hco/3/GRCh38#186119276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22266257-C-A

186119276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266257-C-T

http://identifiers.org/hco/3/GRCh38#186119372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22266322-A-C

186119372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266322-A-G

186119686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266565-G-T

186119770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22266648-A-T

186121244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267373-T-G

186121263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267393-G-A

186121278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267420-T-G

186121310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267450-G-T

186121330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267470-T-A

186121330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267470-T-C

186121409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267538-G-A

186121525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267648-T-A

186121545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267668-T-G

186121767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267916-A-G

186121782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22267932-G-T

186121959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268107-G-T

186122005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268198-C-T

186122062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268315-A-G

186122460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268679-G-A

186122519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268738-A-G

186122606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268934-T-C

186122648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22268967-G-A

186123085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270053-A-G

186123194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270164-C-T

186124222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270597-C-T

186124253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270624-C-G

http://identifiers.org/hco/3/GRCh38#186124356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22270724-A-C

186124379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270747-G-A

186124379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270747-G-T

186124468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270814-C-T

186124507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22270855-A-G

186125016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22271291-T-C

186125274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271531-G-A

186125292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271554-G-T

186126655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271648-T-A

186126655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271648-T-C

186126655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271648-T-G

186126667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271660-T-G

186126818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22271820-T-G

http://identifiers.org/hco/3/GRCh38#186126904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22271899-C-A

186126970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22271939-G-A

186126970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22271939-G-T

186127064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22272028-C-T

186127137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22272100-G-C

186127180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22272138-C-T

186127727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22272338-T-A

186127735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22272346-T-C

186129209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22273061-C-T

186129222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22273074-G-A

http://identifiers.org/hco/3/GRCh38#186129333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22273246-C-A

186129367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22273285-T-C

186131072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22274082-G-A

186131463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22274473-G-T

186131882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22274841-A-G

186132338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22275246-A-T

186132559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22275449-T-C

186132677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22275548-C-T

186138424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276621-G-C

186138448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276644-G-A

186138448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276644-G-C

186138494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276687-G-T

186138581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276751-C-T

186138585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276755-C-T

186138785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276936-A-G

186138833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22276984-G-A

186138857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277008-G-A

186138857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277008-G-T

http://identifiers.org/hco/3/GRCh38#186139070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22277209-C-A

186139070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277209-C-T

http://identifiers.org/hco/3/GRCh38#186139177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22277320-C-A

186139328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277475-C-T

186139464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277610-A-T

186139681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277676-G-T

186139882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22277713-T-G

http://identifiers.org/hco/3/GRCh38#186140117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22277938-C-A

186140194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22278013-T-C

186140565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22278064-G-A

186140613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22278111-C-T

186140639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22278130-G-A

186140639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22278130-G-C

186141587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22279326-C-T

186141647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22279546-G-A

186141794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22279679-A-G

186142823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22280675-C-G

186142825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22280677-G-C

186142825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22280677-G-T

186142960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22280808-T-A

186143199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22280990-G-A

186143199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22280990-G-T

186143530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22281301-C-T

186145295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22282690-G-A

186145560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22282896-T-C

186145742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22283055-G-A

186145742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22283055-G-C

186146298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22284365-G-A

186146814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22284915-G-A

186147156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22285277-A-T

186147241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285358-T-C

186147262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285379-T-C

186147270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285387-A-G

186147339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285452-G-T

186147409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285526-C-T

186147481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285598-G-T

186147670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285724-C-G

186147679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285733-T-C

186147792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285836-A-G

186147864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285908-G-T

186147939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22285979-A-G

186147966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286003-A-T

186147992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286036-G-T

http://identifiers.org/hco/3/GRCh38#186148042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22286091-C-A

http://identifiers.org/hco/3/GRCh38#186148138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22286176-A-C

186148138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286176-A-G

186148154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286192-G-A

186148154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286192-G-T

186148379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286415-G-T

http://identifiers.org/hco/3/GRCh38#186148396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22286432-C-A

186148396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286432-C-T

http://identifiers.org/hco/3/GRCh38#186148431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22286466-C-A

186148455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286493-A-G

186148637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286679-C-T

186148642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286684-G-A

186148863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286862-G-C

186148863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22286862-G-T

186149067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287025-A-G

186149131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287090-T-C

186149155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287114-C-T

186149248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287217-C-T

186149275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287244-C-G

186149361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287332-G-A

186149361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287332-G-T

186149367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287338-C-T

http://identifiers.org/hco/3/GRCh38#186149450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22287406-C-A

186149567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287522-T-A

186149567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287522-T-C

http://identifiers.org/hco/3/GRCh38#186149585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22287540-A-C

186149585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287540-A-G

186149585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287540-A-T

186149595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287550-G-T

186149604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287559-A-G

186149604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 22287559-A-T

http://identifiers.org/hco/3/GRCh38#186149861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22287793-C-A

http://identifiers.org/hco/3/GRCh38#186150212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22288119-A-C

186150272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22288181-C-G

186150272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22288181-C-T

186150299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22288207-G-A

186150299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22288207-G-T

186150601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22288534-C-T

186151428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22289311-G-A

186151428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22289311-G-T

186151519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22289392-A-G

186153384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22290004-C-T

186153719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22290275-C-T

186154765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22290963-C-T

http://identifiers.org/hco/3/GRCh38#186154907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22291084-C-A

186154993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22291169-T-A

186161518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22298028-T-C

186161518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22298028-T-G

186161633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22298146-A-G

186161678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298191-A-T

186161761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298274-G-T

186161794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298302-G-A

186161794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298302-G-T

186161810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298317-A-G

186162290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298467-C-T

186162330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298505-G-A

186162453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22298629-A-G

186162474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298650-A-G

186163395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22298868-G-A

186163596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299065-C-T

186163619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299092-G-T

http://identifiers.org/hco/3/GRCh38#186163712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22299182-A-C

186163752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299219-G-A

186163769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299236-G-T

186163801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299268-T-C

186163995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299461-C-T

186164160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299606-T-C

http://identifiers.org/hco/3/GRCh38#186164271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22299714-C-A

186164461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22299890-A-G

186164700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300060-T-C

http://identifiers.org/hco/3/GRCh38#186164761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22300505-C-A

186164761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300505-C-T

186164778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300522-A-G

186164778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300522-A-T

186164796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300540-A-G

186164936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22300689-T-C

186165053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300804-A-G

http://identifiers.org/hco/3/GRCh38#186165138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22300880-A-C

186165138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300880-A-T

186165218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22300953-T-C

http://identifiers.org/hco/3/GRCh38#186165219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22300954-A-C

186165604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22301306-T-G

186165892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22301579-A-T

186165935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22301656-T-A

186165973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22301694-T-C

186166309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22301963-G-A

186166743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22302384-G-C

186166759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22302400-A-G

186166759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22302400-A-T

186167029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22302817-T-C

186167836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22303622-G-A

186168019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22303792-T-A

186168284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22303998-G-C

186168535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22304195-T-C

186168837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22304313-G-A

186169338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22304846-T-A

186169422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22304922-T-C

http://identifiers.org/hco/3/GRCh38#186169464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22304967-A-C

http://identifiers.org/hco/3/GRCh38#186169784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22305053-C-A

186170007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22305255-A-G

186170109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22305343-A-T

186173183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22307067-C-T

http://identifiers.org/hco/3/GRCh38#186173346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22307206-C-A

186173588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22307427-G-A

186173754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22307563-G-A

186174787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308063-A-G

http://identifiers.org/hco/3/GRCh38#186175162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22308397-C-A

186175452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308659-G-C

186175541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308757-T-C

186176780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308992-G-T

186176795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309007-G-A

186176920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309125-G-A

186177052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309251-T-C

186177070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309269-G-A

186177094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309292-C-T

http://identifiers.org/hco/3/GRCh38#186177446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22309430-A-C

http://identifiers.org/hco/3/GRCh38#186177608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22309601-C-A

186177608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309601-C-T

186177761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309767-T-C

186177896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22310011-C-T

http://identifiers.org/hco/3/GRCh38#186178448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22310531-A-C

186178572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22310652-G-A

186178747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22310817-G-A

186178792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22310862-C-T

186178855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22310920-T-C

186178887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22310953-A-G

186178994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311052-C-T

186179073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311110-G-T

186179171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311199-A-G

186179466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311483-C-T

186179527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311509-A-T

186179676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311668-G-A

186179796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311756-G-A

186179835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22311786-C-T

186180296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22312218-C-T

http://identifiers.org/hco/3/GRCh38#186180419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22312339-A-C

186180542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22312535-A-G

186180748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22312954-T-C

186180787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22312993-G-A

186180986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22313238-C-T

186180987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22313239-G-A

186181267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22313466-G-A

186181331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22313527-C-T

186181940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22313751-T-C

http://identifiers.org/hco/3/GRCh38#186182037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22313836-C-A

186182999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315133-A-G

http://identifiers.org/hco/3/GRCh38#186183012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22315146-A-C

186183082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315225-A-T

186183166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315308-C-G

186183244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315390-T-C

186183256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315402-A-G

186183423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315547-T-C

186183477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22315594-G-A

186184028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316021-G-A

186184110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316089-C-T

186184187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316159-A-G

186184369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316332-T-C

http://identifiers.org/hco/3/GRCh38#186184721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22316412-C-A

186184770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316447-C-T

186184839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316520-A-G

186185071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316726-G-T

http://identifiers.org/hco/3/GRCh38#186185092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22316747-C-A

186185101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316756-G-A

186185106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316761-A-T

186185169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22316800-A-G

186185602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317203-C-T

186185619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317220-A-G

186186139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317448-C-T

186186234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317525-A-G

186186563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317712-C-T

186186650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317799-G-T

186186654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317803-T-C

186186655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317804-G-A

186186763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317909-G-A

http://identifiers.org/hco/3/GRCh38#186186787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22317932-A-C

186186787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317932-A-T

186186840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22317955-T-C

http://identifiers.org/hco/3/GRCh38#186186919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22318019-C-A

186186919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318019-C-T

186186989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318085-G-A

186187089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318188-G-A

186187165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318259-C-G

186187807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318582-G-A

186187866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318642-A-G

186188112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318874-T-C

186188115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318877-G-C

186188115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22318877-G-T

186188374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22319146-A-G

186188470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22319200-G-A

186188472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22319202-A-G

http://identifiers.org/hco/3/GRCh38#186188496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22319226-C-A

http://identifiers.org/hco/3/GRCh38#186188502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22319232-C-A

186188502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22319232-C-T

186189044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22319526-A-T

186189364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22319739-C-G

186189439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22319829-C-T

186190136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22320580-C-T

186190166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22320610-T-C

186190413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22320828-T-C

186190445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22320861-C-T

186190458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22320873-A-T

186190676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321052-T-A

186190676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321052-T-C

186190730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321096-C-T

186190735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321101-G-C

186190794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321149-G-A

186191158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321435-A-G

186191181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321458-G-A

186191244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321531-C-T

186191374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321636-T-C

186191461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321724-C-T

186191551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321810-T-C

186191571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321830-T-C

186191571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321830-T-G

186191593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321853-C-T

186192063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322390-G-A

186192564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322921-T-C

186192776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323097-G-A

186192776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323097-G-T

http://identifiers.org/hco/3/GRCh38#186193277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22323423-C-A

186193567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323642-G-A

186193663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323721-G-A

http://identifiers.org/hco/3/GRCh38#186193741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22323786-C-A

186193741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323786-C-G

186193814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323836-G-A

http://identifiers.org/hco/3/GRCh38#186193906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22323918-C-A

186193907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22323919-G-T

http://identifiers.org/hco/3/GRCh38#186193933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22323945-C-A

186194050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22324043-G-A

186194118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22324133-G-A

186194193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22324191-G-C

186194349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22324337-G-C

186194522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22324488-T-C

186197154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325088-G-C

186197308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325202-T-A

http://identifiers.org/hco/3/GRCh38#186197370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22325255-C-A

186197417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325287-C-T

186197465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325385-G-A

186197612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325506-G-T

186197869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325756-C-T

186197889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22325775-A-G

186198154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326024-G-A

186198224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326093-T-C

186198416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326238-G-A

186198689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326498-C-T

186199443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326850-T-C

186199446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326853-C-G

186199494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326900-C-G

186199494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326900-C-T

186199498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326904-A-G

186199498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326904-A-T

186199855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326955-G-A

186199855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22326955-G-T

186199976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327062-G-A

186199976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327062-G-C

186200108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327331-G-T

186200130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327352-A-G

186200357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327533-T-G

186200461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327624-C-T

186200573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327728-C-T

186200718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327869-G-A

186200770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327923-T-C

186200782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327935-G-A

186200782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22327935-G-T

186201135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22328291-A-G

186201216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22328348-G-C

186201235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22328367-A-G

186201279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22328410-C-T

186201795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22328889-T-C

186201884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22328975-G-A

186201923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22329014-A-G

http://identifiers.org/hco/3/GRCh38#186202009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22329098-A-C

186202085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22329242-G-T

186202469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22329589-T-C

186203079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330157-A-G

186203168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330242-C-T

186203207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330279-A-G

186203208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330280-C-T

186203254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330326-T-C

186203589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330781-C-T

186203598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22330790-T-C

http://identifiers.org/hco/3/GRCh38#186203929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22331061-C-A

186203929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22331061-C-T

186205925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22333346-A-T

186206096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22333526-A-G

186206548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22333665-G-T

http://identifiers.org/hco/3/GRCh38#186206600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22333709-C-A

186206600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22333709-C-G

186206603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22333712-C-T

186207408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22334083-C-T

186207409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22334084-A-G

http://identifiers.org/hco/3/GRCh38#186207432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22334101-A-C

186207432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22334101-A-G

186207439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22334107-G-C

186207602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22334231-T-C

http://identifiers.org/hco/3/GRCh38#186207667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22334296-A-C

186208580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22335181-G-A

186208581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22335182-T-C

186208762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22335381-G-T

186209559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22336094-G-A

186209808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22336298-C-T

186209893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22336378-C-T

186210004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22336471-G-A

http://identifiers.org/hco/3/GRCh38#186210015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22336489-C-A

186210123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22336603-G-C

186210505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22336977-G-A

186210846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337291-C-G

186210846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337291-C-T

http://identifiers.org/hco/3/GRCh38#186210912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22337349-C-A

186210944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337386-G-A

186210944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337386-G-C

186211023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337442-G-T

186211058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337463-G-C

186211060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337465-G-A

186211061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337466-C-T

186211386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22337979-C-G

186211607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338107-T-C

186211669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338162-G-C

186211669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338162-G-T

186211722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338230-C-T

186211738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338255-G-T

186211782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338278-C-T

186211908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338408-G-A

186211908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338408-G-C

186211908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338408-G-T

186212092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338594-A-G

186212314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338805-T-C

186212388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338877-C-T

http://identifiers.org/hco/3/GRCh38#186212433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22338924-A-C

186212441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22338932-G-C

186212593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339077-A-T

186213010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339436-A-G

http://identifiers.org/hco/3/GRCh38#186213023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22339445-C-A

186213023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339445-C-G

186213075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339495-G-T

186213145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339565-A-G

186213218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339627-T-G

186213228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339637-G-A

186213397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339801-A-T

186213414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339818-A-G

186213436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339839-T-C

http://identifiers.org/hco/3/GRCh38#186213556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22339959-A-C

186213556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22339959-A-T

186213589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340004-G-A

186213677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340070-G-A

186213781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340174-T-C

186213885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340275-C-T

186213911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340286-A-G

186213938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340313-A-G

186214254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340608-G-A

186214344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340696-G-A

186214400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340703-C-T

186214490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340779-T-C

186214704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22340982-G-A

186216343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22343439-G-C

186216370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22343457-A-G

186216402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22343490-C-G

186216417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22343505-C-T

186216562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22344059-G-A

186216599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22344091-G-A

http://identifiers.org/hco/3/GRCh38#186216713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22344196-C-A

186217071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22344508-G-C

186217142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22344570-T-A

186217203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22344642-C-T

186217399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22344829-C-T

186217504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

186217629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22345022-C-T

186217639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22345032-G-C

186217880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22345279-A-G

http://identifiers.org/hco/3/GRCh38#186219131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22346169-C-A

186219405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22346415-G-A

186219602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22346609-T-C

186219737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22346753-G-C

186219853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22346866-T-C

186220276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349289-A-G

http://identifiers.org/hco/3/GRCh38#186220393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22349405-A-C

186220420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349431-G-T

186220483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349517-G-C

186220511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349545-T-C

186220804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349770-G-A

186220804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349770-G-C

186220831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349798-C-G

186220905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349871-C-T

186221002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22349947-C-T

186221025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22350040-G-A

186221097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350183-C-T

186221155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350294-G-A

186221216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350358-G-A

186221222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350364-C-T

http://identifiers.org/hco/3/GRCh38#186221237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22350379-C-A

186221237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350379-C-T

186221248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350390-G-T

186221634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350665-C-T

186221635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350666-C-T

186221642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350673-C-T

186221649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350680-C-G

186221810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350836-G-C

186221881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350896-C-T

186221969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22350980-T-C

186222011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351019-T-C

186222368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351301-C-T

186222372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351305-C-T

186223085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351536-T-C

186223296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351727-A-T

186223419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351843-G-A

186223438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351860-G-T

186223575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351989-C-G

186223575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22351989-C-T

186223651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22352121-C-G

186223651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22352121-C-T

http://identifiers.org/hco/3/GRCh38#186223667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22352136-A-C

http://identifiers.org/hco/3/GRCh38#186223719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22352187-C-A

186223755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22352223-C-T

186223982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22352409-G-A

186224235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22352647-C-T

186225369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354365-T-C

http://identifiers.org/hco/3/GRCh38#186225377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22354373-C-A

186225377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354373-C-G

186225377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354373-C-T

186225425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354421-C-T

186225431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354427-C-T

186225479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354475-C-T

186225565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354569-G-A

186225629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354644-G-A

186225715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354744-T-C

186225747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354777-T-C

186225864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22354880-C-T

186226157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22355026-A-G

186226367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22355224-G-T

186226688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22355512-T-C

186226758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22355582-C-T

186226851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22355673-C-T

186227100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22355894-T-C

http://identifiers.org/hco/3/GRCh38#186227467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22356237-A-C

186227662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22356408-A-G

186232259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22358609-T-G

http://identifiers.org/hco/3/GRCh38#186232325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22359208-C-A

186232537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22359413-G-A

186232627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22359479-T-C

http://identifiers.org/hco/3/GRCh38#186232830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22359699-C-A

186233046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22359885-C-G

http://identifiers.org/hco/3/GRCh38#186233096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22359933-C-A

186233096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22359933-C-T

186233097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22359934-G-A

186233097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22359934-G-T

http://identifiers.org/hco/3/GRCh38#186233247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22360073-A-C

186235215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22360141-T-C

186235303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22360232-T-C

186235308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22360237-G-T

186235829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22360782-C-T

186235939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22360921-T-C

186235942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22360924-C-T

http://identifiers.org/hco/3/GRCh38#186235951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22360933-A-C

186236041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22361053-G-A

186236049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22361060-A-G

186236671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22361641-C-T

http://identifiers.org/hco/3/GRCh38#186236760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22361738-A-C

186236772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22361746-G-T

186236781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22361755-C-T

186236909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22361890-C-T

186237136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362100-T-A

186237191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362160-C-T

http://identifiers.org/hco/3/GRCh38#186237200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22362169-C-A

186237323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362292-T-C

186237569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362527-A-G

186237569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362527-A-T

186237578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362536-A-G

186237794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362743-T-C

186237830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362759-C-T

186237908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362849-A-T

186237911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362852-C-T

186237990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22362929-T-A

186238778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363541-T-G

186238822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363584-A-T

186238895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363656-T-C

186238901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363662-C-G

186239022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363745-C-T

186239063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363787-T-A

186239063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363787-T-C

186239114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363835-G-A

186239114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363835-G-T

186239178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22363874-C-T

186239366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364044-T-C

186239638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22364343-C-T

186240087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364741-G-A

186240093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364747-A-G

186240158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364801-A-T

186240165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364808-C-T

186240208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364867-C-T

186240209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22364868-G-A

186240323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365007-G-A

186240403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22365094-T-C

186241162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22366521-G-A

186241796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22366789-G-T

186242332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22367211-T-C

186242464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22367359-A-G

186242496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22367389-C-T

http://identifiers.org/hco/3/GRCh38#186242677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22367568-C-A

186242678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22367569-T-C

http://identifiers.org/hco/3/GRCh38#186242732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#22367595-A-C

186242732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22367595-A-G

186242732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22367595-A-T

186242746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22367609-G-A

186242746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22367609-G-T

186242766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22367631-A-G

186244172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369358-G-C

186244182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369368-A-G

186244197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369384-G-A

186244236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369437-C-G

186244252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369453-T-C

186244353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369555-T-C

186244353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369555-T-G

186244405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369590-A-T

186245033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22369927-G-A

186245380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370266-T-A

186245380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370266-T-C

186245450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370348-A-G

186245529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370381-G-A

186245709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370582-C-G

186245709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370582-C-T

186245778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370652-C-T

186245798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370672-T-C

186245809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370683-C-G

186245809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370683-C-T

186246349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370842-T-C

186246403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22370890-T-G

http://identifiers.org/hco/3/GRCh38#186246627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22371098-C-A

186246627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22371098-C-T

186246749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22371193-T-C

186246816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22371259-A-T

http://identifiers.org/hco/3/GRCh38#186246876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22371288-A-C

186247290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22371694-G-A

186247431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22371786-G-T

186247488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22371847-C-T

186247771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372127-T-C

186247785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372141-G-T

186247972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372261-C-T

186247977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372266-T-C

186247991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372280-C-T

186248091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372355-G-A

186248091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372355-G-T

186248519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372686-T-C

186248532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372699-G-C

186248725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372885-G-C

186248725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372885-G-T

186248795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372923-A-G

186248870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372949-G-C

186248913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22372976-C-T

186249155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22373069-G-A

186249156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22373075-G-A

186249317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22373216-T-C

186251148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22374566-A-G

http://identifiers.org/hco/3/GRCh38#186251182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22374599-A-C

186251274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22374681-G-A

186251403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22374794-T-C

186251567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22374928-A-G

186251567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22374928-A-T

186251694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375031-A-G

186251742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375059-A-G

186251743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375060-T-A

http://identifiers.org/hco/3/GRCh38#186251933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22375250-C-A

http://identifiers.org/hco/3/GRCh38#186251947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22375264-C-A

186251947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375264-C-G

186251947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375264-C-T

186251959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375276-G-A

186252012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375296-A-G

186252012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375296-A-T

186252016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375300-G-T

186252037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375319-G-C

186252037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375319-G-T

186252054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375336-A-T

186252131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375437-G-A

186252134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22375440-G-T

186252531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376428-C-T

186252771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376656-G-A

http://identifiers.org/hco/3/GRCh38#186252774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22376659-C-A

186253032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376706-G-A

186253032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376706-G-C

186253037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376711-T-A

186253037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376711-T-C

186253075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376749-A-G

186253178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22376852-C-T

http://identifiers.org/hco/3/GRCh38#186253195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22376869-C-A

186253246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376913-T-A

http://identifiers.org/hco/3/GRCh38#186253302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22376967-A-C

186253302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376967-A-G

186253306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22376971-T-C

http://identifiers.org/hco/3/GRCh38#186253316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22376981-C-A

http://identifiers.org/hco/3/GRCh38#186253318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22376983-C-A

186253701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377264-A-G

186254173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377688-G-T

186254203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377700-G-A

186254272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377750-C-G

186254272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22377750-C-T

186254645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378059-C-T

186254714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378104-C-T

http://identifiers.org/hco/3/GRCh38#186254743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22378128-C-A

186254743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378128-C-T

186255103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378408-G-T

http://identifiers.org/hco/3/GRCh38#186255148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22378432-A-C

186255444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378646-C-T

186255615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378785-G-A

186255813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22378932-G-A

186255813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22378932-G-C

186255813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22378932-G-T

186255867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22378983-A-G

http://identifiers.org/hco/3/GRCh38#186255873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#22378989-C-A

186255873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22378989-C-G

186255873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22378989-C-T

186256085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22379193-G-A

186256680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380180-C-T

186256822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380350-C-T

186257159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22380782-C-T

http://identifiers.org/hco/3/GRCh38#186257517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22381174-C-A

186257517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381174-C-T

186257530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381190-G-A

186257654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381280-G-C

186257654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381280-G-T

186257655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381281-G-A

http://identifiers.org/hco/3/GRCh38#186257702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22381297-C-A

186257702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381297-C-T

http://identifiers.org/hco/3/GRCh38#186257891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22381485-A-C

186257891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22381485-A-G

186257912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22381506-G-A

http://identifiers.org/hco/3/GRCh38#186258043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22381906-A-C

186258064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381927-G-T

186258079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381942-T-C

186258120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22381984-G-C

186258209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382094-C-T

186258210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382095-T-C

186258746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382627-G-A

186258746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382627-G-C

186258792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382674-A-G

186258869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382759-G-T

http://identifiers.org/hco/3/GRCh38#186259009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22382876-C-A

186259009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382876-C-G

186259040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382906-C-G

186259049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22382914-T-C

186259309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22383159-G-A

186259310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22383160-G-C

http://identifiers.org/hco/3/GRCh38#186259346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22383189-C-A

186259346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22383189-C-T

186259501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22383339-T-C

186259815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22383595-T-A

186260093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22383788-T-C

186260097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22383792-G-A

186260422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384025-G-T

186260474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22384072-T-C

186260575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384155-G-T

186260576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384156-A-T

http://identifiers.org/hco/3/GRCh38#186260583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22384163-A-C

186260583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384163-A-T

186260610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384189-T-A

186260650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384228-G-A

186260825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384378-T-C

186260827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384380-A-G

186260860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384409-T-C

186260881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384430-C-G

186261320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384791-G-A

186261357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384829-A-G

186261390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384867-A-G

186261400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384877-A-G

186261410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384887-G-A

186261410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384887-G-C

186261471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384943-G-A

186261471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22384943-G-T

186261539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385020-G-A

186261539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385020-G-C

186261572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385052-G-A

186261572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385052-G-C

186261590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385059-G-T

186261591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385060-G-A

186261591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385060-G-T

186261600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385069-T-G

186261637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385106-G-A

186261637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385106-G-T

186261645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385114-G-A

http://identifiers.org/hco/3/GRCh38#186261655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22385125-C-A

186261655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385125-C-G

186261655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385125-C-T

186261758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22385224-C-G

186261758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22385224-C-T

186261901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22385350-T-A

186261901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22385350-T-C

186261911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22385360-G-A

186261911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22385360-G-C

186261911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22385360-G-T

186261927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22385375-G-T

186261974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385419-T-C

186262028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385467-G-C

186262028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385467-G-T

http://identifiers.org/hco/3/GRCh38#186262071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22385489-C-A

186262215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385791-G-A

186262342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22385906-C-T

http://identifiers.org/hco/3/GRCh38#186262386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22385956-C-A

http://identifiers.org/hco/3/GRCh38#186262502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22386065-C-A

186262502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386065-C-T

186262674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386203-A-G

186262803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22386329-C-T

186263680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387116-G-A

186263680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387116-G-T

186263715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387148-G-T

186263804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387222-G-A

186263857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387275-A-G

186264391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22387973-G-A

186264438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388016-A-G

http://identifiers.org/hco/3/GRCh38#186264472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22388048-C-A

186264484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388061-G-A

186264485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388062-A-G

http://identifiers.org/hco/3/GRCh38#186264803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22388481-C-A

186265005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388668-G-A

186265123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388791-T-A

186265123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388791-T-C

186265123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388791-T-G

186265143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388810-G-A

186265143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22388810-G-T

http://identifiers.org/hco/3/GRCh38#186265156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22388823-A-C

186265418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22389086-T-A

186265418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22389086-T-C

186265418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22389086-T-G

186267296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390229-C-T

186267319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390249-A-G

http://identifiers.org/hco/3/GRCh38#186267351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22390278-C-A

186267356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390283-C-T

186267848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390590-T-C

186267854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390596-G-T

186267912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390649-A-G

186268169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390840-T-C

186268169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390840-T-G

186268184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22390855-T-C

186268448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391110-C-T

186268564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391157-A-G

186268616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391169-G-A

186268675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391219-G-A

186268675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391219-G-T

186268714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391263-C-T

186268761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391310-A-G

186268761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391310-A-T

186268782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391331-G-A

186268782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391331-G-T

186268971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391519-G-T

http://identifiers.org/hco/3/GRCh38#186269189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22391702-A-C

186269221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391726-T-C

186269325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391830-G-A

186269478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391955-G-A

186269485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391962-T-A

186269508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391963-T-A

186269508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22391963-T-C

186269550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392008-A-G

186269585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392040-C-G

186269585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392040-C-T

186269800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392096-G-A

186269957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392237-A-G

http://identifiers.org/hco/3/GRCh38#186270070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22392330-C-A

186270070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392330-C-T

186270785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22392724-G-A

186271138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393027-C-G

186271310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393167-C-G

186271355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393216-C-T

186271378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393239-T-C

186271485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393315-C-T

186271494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393329-A-G

186271540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393376-C-T

186271658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393482-G-A

186271768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393591-G-A

186271903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393710-G-T

186272115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393924-G-A

186272115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393924-G-T

186272116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393925-G-A

186272116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393925-G-T

186272131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393937-G-A

186272131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393937-G-T

186272191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22393997-C-T

186272230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22394037-G-T

186272330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22394137-A-G

186272388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22394191-T-C

http://identifiers.org/hco/3/GRCh38#186272419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22394236-C-A

http://identifiers.org/hco/3/GRCh38#186272478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22394266-C-A

http://identifiers.org/hco/3/GRCh38#186272557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22394323-C-A

186273933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22394883-G-A

http://identifiers.org/hco/3/GRCh38#186274007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22394955-A-C

186274007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22394955-A-T

186274063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395008-T-C

186274066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395011-C-T

186275287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395215-T-C

http://identifiers.org/hco/3/GRCh38#186275439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22395347-C-A

186275439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395347-C-T

http://identifiers.org/hco/3/GRCh38#186275465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22395373-C-A

186275465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395373-C-G

186275465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395373-C-T

186275529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395419-T-G

186275681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395570-A-G

186275692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395583-C-G

186275692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395583-C-T

186275699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395590-G-A

186275733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395619-C-T

186275751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395648-T-C

186275769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395668-G-A

186275769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22395668-G-T

186276218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22396184-T-A

186276218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22396184-T-C

186278110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22396972-A-G

186278125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22396987-C-T

http://identifiers.org/hco/3/GRCh38#186279241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22397753-C-A

186279304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397814-T-C

186279304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397814-T-G

http://identifiers.org/hco/3/GRCh38#186279316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22397822-C-A

186279316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397822-C-T

http://identifiers.org/hco/3/GRCh38#186279341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22397844-C-A

186279365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397868-G-A

http://identifiers.org/hco/3/GRCh38#186279413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22397912-C-A

186279413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397912-C-T

http://identifiers.org/hco/3/GRCh38#186279414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22397913-C-A

186279414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397913-C-T

http://identifiers.org/hco/3/GRCh38#186279444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22397941-C-A

186279444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22397941-C-T

186279483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22398151-C-T

http://identifiers.org/hco/3/GRCh38#186279518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22398184-A-C

http://identifiers.org/hco/3/GRCh38#186279559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22398223-C-A

186279559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22398223-C-T

186279793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22398455-A-G

186279842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22398484-T-C

186279941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22398583-G-A

186279999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398642-G-A

http://identifiers.org/hco/3/GRCh38#186280002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22398645-C-A

186280002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398645-C-T

186280023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398661-T-G

186280073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398707-T-C

http://identifiers.org/hco/3/GRCh38#186280083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22398717-C-A

186280083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398717-C-G

186280100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398734-G-A

186280100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22398734-G-T

http://identifiers.org/hco/3/GRCh38#186280116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22398750-C-A

http://identifiers.org/hco/3/GRCh38#186280149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22398792-C-A

http://identifiers.org/hco/3/GRCh38#186280498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22399112-C-A

186280498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399112-C-T

186280535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399150-G-A

186280535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399150-G-T

http://identifiers.org/hco/3/GRCh38#186280614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22399233-C-A

186280614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399233-C-T

186280694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22399297-C-T

http://identifiers.org/hco/3/GRCh38#186280786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22399388-C-A

186280786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399388-C-T

186280796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399427-T-C

186280861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399494-G-C

186280861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399494-G-T

186280871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399500-T-C

186280886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399515-G-A

186280886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399515-G-T

186280899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399525-T-G

186280991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399634-G-C

http://identifiers.org/hco/3/GRCh38#186281115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22399742-C-A

186281265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399906-T-A

186281265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399906-T-G

186281336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22399971-T-A

186281475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22400111-A-G

186281522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22400158-C-G

186281522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22400158-C-T

186281554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22400189-G-A

186281689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22400938-G-C

186281820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401046-G-A

186282083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401284-A-T

186282086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401287-C-T

186282157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401350-C-G

186282196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401389-C-T

186282223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401416-C-T

http://identifiers.org/hco/3/GRCh38#186282307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22401474-C-A

186282307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401474-C-T

186282332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401499-A-G

186283555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22401998-T-C

186283806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22402411-G-A

186283904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22402612-C-T

186283918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22402626-A-G

186284268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22402807-C-T

http://identifiers.org/hco/3/GRCh38#186284271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22402810-C-A

http://identifiers.org/hco/3/GRCh38#186284439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22402965-A-C

186284451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22402979-C-T

186284501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403029-A-G

http://identifiers.org/hco/3/GRCh38#186284792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22403312-A-C

186284792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403312-A-G

http://identifiers.org/hco/3/GRCh38#186284838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22403350-C-A

186284838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403350-C-T

186284889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403398-G-C

186284911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403425-G-C

186285025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403516-G-A

186285189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22403687-T-C

186286272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22404692-T-G

186286610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22404966-T-G

186286635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22404992-A-G

186287112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405176-T-A

186287133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405196-G-A

186287150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405213-A-G

http://identifiers.org/hco/3/GRCh38#186287455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22405473-A-C

186287515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405546-G-A

http://identifiers.org/hco/3/GRCh38#186287516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22405547-C-A

186287551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405582-A-G

186287626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405646-T-A

186287690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22405710-T-C

186288204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406299-G-A

186288272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406381-A-G

186288418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406801-G-A

186288483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406853-G-A

186288483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406853-G-C

186288490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406860-A-T

http://identifiers.org/hco/3/GRCh38#186288566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22406931-A-C

186288566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406931-A-T

186288624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406966-T-A

186288630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406972-G-A

186288630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22406972-G-T

186288736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22407075-G-A

186288736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22407075-G-C

186288736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22407075-G-T

186288744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22407083-C-G

186288793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22407132-G-A

186288813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22407152-G-A

186288813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22407152-G-C

186288813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22407152-G-T

http://identifiers.org/hco/3/GRCh38#186288913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22407250-A-C

186288913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407250-A-T

186288937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407273-C-G

http://identifiers.org/hco/3/GRCh38#186289190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22407519-C-A

186289227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407552-A-G

186289232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22407557-T-C

186290273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22412006-G-A

186290454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22412227-A-T

186290797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22412550-T-C

186290856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22412605-G-C

186290900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22412642-T-C

186291569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22413300-G-A

http://identifiers.org/hco/3/GRCh38#186291636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22413362-C-A

186291636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22413362-C-G

186292202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22413867-T-C

186292202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22413867-T-G

186292774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22414313-C-T

186292806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22414351-T-A

186292972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22414510-T-C

186293125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22414661-A-G

186293287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22414812-C-T

186293381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22414938-G-A

186293593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415108-C-T

186293655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415176-G-A

186293908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415443-G-A

186293921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415456-C-G

186293947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415483-C-T

186293964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415523-G-T

186294019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415590-T-A

186294148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22415723-G-A

186295607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22416893-T-A

186295607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22416893-T-C

186295607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22416893-T-G

186295632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22416915-G-A

186295632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22416915-G-T

http://identifiers.org/hco/3/GRCh38#186295635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22416918-C-A

186295749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417000-T-A

186295764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417015-C-G

186295790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417041-G-T

186296245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417395-T-C

186296282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417440-G-A

186296293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417451-G-A

186296427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417559-A-G

186296428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417560-T-A

186296520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417637-G-A

186296794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417872-T-C

186296826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417904-G-A

186296907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22417984-T-C

186296986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418078-C-T

186297018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418159-C-T

186297059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418257-C-G

186297326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418516-T-C

186297498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418652-G-A

186297498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418652-G-T

http://identifiers.org/hco/3/GRCh38#186297542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22418699-C-A

186297542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418699-C-T

http://identifiers.org/hco/3/GRCh38#186297560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22418717-A-C

186297560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418717-A-G

186297560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418717-A-T

186297621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418776-G-A

186297621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418776-G-C

186297621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418776-G-T

http://identifiers.org/hco/3/GRCh38#186297622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22418777-C-A

186297762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418880-C-T

186297785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22418903-C-T

186297946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419070-G-A

186297946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419070-G-T

http://identifiers.org/hco/3/GRCh38#186297970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22419093-A-C

186297999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419121-C-G

186298004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419126-G-A

186298004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419126-G-T

186298006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419128-T-C

186298075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22419200-G-A

186298075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22419200-G-T

186298101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22419226-C-T

186298114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22419239-G-A

186298114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 22419239-G-T

186298261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419386-A-G

186298264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419389-G-A

186298314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419440-G-A

186298314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419440-G-T

http://identifiers.org/hco/3/GRCh38#186298315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22419441-C-A

186298315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419441-C-G

186298315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419441-C-T

186298509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22419599-G-T

186298580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22420896-G-A

186298619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22420928-C-G

186298767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421057-T-A

http://identifiers.org/hco/3/GRCh38#186299209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22421464-C-A

186299209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421464-C-T

186299303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22421558-T-C

186300319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22422898-C-T

http://identifiers.org/hco/3/GRCh38#186300328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22422907-C-A

186300480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423062-T-C

186300557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423137-G-A

186300756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22423289-A-G

186300943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22424317-A-G

186301122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22424468-C-T

186301645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22424937-T-C

186301702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22425001-T-G

186301716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22425016-T-C

186301777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22425072-A-G

186301885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22425192-C-T

186302144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22425428-G-A

http://identifiers.org/hco/3/GRCh38#186302182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22425460-C-A

186302676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22425847-G-A

186303266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22426395-G-T

186303390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22426481-G-T

186303783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22426822-A-G

186303808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22426841-T-C

186304062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22427098-C-G

186304278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22427304-G-T

http://identifiers.org/hco/3/GRCh38#186304605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22427582-A-C

http://identifiers.org/hco/3/GRCh38#186304699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22427657-C-A

186304759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22427722-T-A

186304759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22427722-T-C

186305267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428208-T-A

186305283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428224-G-C

186305321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428262-T-A

186305325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428264-C-T

186305326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428265-T-C

186305356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428305-G-A

186305423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428370-C-T

186305443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428389-G-A

http://identifiers.org/hco/3/GRCh38#186305508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22428434-A-C

186305588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428475-G-T

186305695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428566-C-T

186305716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428582-G-A

186305821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428682-A-G

186305864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428724-C-T

186305998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428844-T-C

186306059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428890-T-A

186306149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22428969-C-G

186306321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22429062-A-G

186306473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22429180-G-A

186306665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22429319-G-A

186306665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22429319-G-T

http://identifiers.org/hco/3/GRCh38#186306675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22429331-A-C

186306682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22429338-G-C

186306682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22429338-G-T

186306726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22429370-T-A

186306726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22429370-T-C

186306727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22429371-G-A

http://identifiers.org/hco/3/GRCh38#186306756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22429403-C-A

http://identifiers.org/hco/3/GRCh38#186306829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22429475-A-C

186306829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22429475-A-G

186306886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22429514-T-C

186306887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 22429515-G-T

186306893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22429521-G-A

186306893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 22429521-G-T

186307331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430035-A-G

186307412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430113-T-C

186307511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430213-A-T

http://identifiers.org/hco/3/GRCh38#186307527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22430227-C-A

186307527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22430227-C-G

186307765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22431385-G-T

186308019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22431615-C-T

186308078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22431670-G-A

186308637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22432222-G-A

186308750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22432340-C-T

186308850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22432427-C-T

186308874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22432451-C-T

186309285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433030-G-C

186309350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433091-T-C

186309444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433183-C-T

186309454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433193-T-C

186309741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433475-T-C

186309755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433487-C-G

186309811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433540-T-C

http://identifiers.org/hco/3/GRCh38#186309984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22433640-C-A

186310003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22433659-T-A

186310470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434423-G-A

186310504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434456-T-C

186310728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434605-A-T

186310741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434618-C-T

186310831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434697-C-T

186310936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434787-G-A

186310936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434787-G-C

186310964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434815-G-T

186311027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22434905-C-G

186311350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435220-G-T

186311369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435241-C-G

186311369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435241-C-T

186311449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435321-T-C

http://identifiers.org/hco/3/GRCh38#186311715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22435565-C-A

186311715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435565-C-T

186311799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435648-G-C

186311799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435648-G-T

186312203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22435751-C-T

186313056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436458-C-G

186313159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436554-T-C

186313159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436554-T-G

186313347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436768-A-G

186313405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436830-A-T

186313431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436856-T-C

http://identifiers.org/hco/3/GRCh38#186313473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22436890-C-A

186313473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436890-C-T

http://identifiers.org/hco/3/GRCh38#186313484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22436901-A-C

186313535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436944-A-G

186313554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436963-G-C

186313566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436975-G-A

186313579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22436988-C-T

186313687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437073-G-A

186313687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437073-G-T

186313754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437139-C-T

186313787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437171-A-G

186313914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437290-T-C

http://identifiers.org/hco/3/GRCh38#186316537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22437454-A-C

186316537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437454-A-G

186316774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437662-G-C

186316999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437887-G-A

http://identifiers.org/hco/3/GRCh38#186317008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22437896-C-A

186317008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22437896-C-T

186317164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438098-T-G

186317179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438110-C-T

186317197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438128-C-T

186317270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438192-G-T

186317420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438338-C-T

186317916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438632-C-T

186318089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438805-A-G

186318368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22438973-T-C

http://identifiers.org/hco/3/GRCh38#186318707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22439330-A-C

186318749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439369-G-T

186318907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439515-T-C

186318941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439552-G-A

186318960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439575-C-T

186319033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439648-C-G

186319033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439648-C-T

186319156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22439731-T-C

http://identifiers.org/hco/3/GRCh38#186319762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22440391-C-A

186319793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440423-G-A

186319793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440423-G-T

186319875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440492-A-G

186319989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440590-T-C

186319993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440594-C-T

186320140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440718-G-A

http://identifiers.org/hco/3/GRCh38#186320251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22440816-C-A

186320251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440816-C-G

186320251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440816-C-T

186320262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440827-A-T

186320281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440846-G-A

186320281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440846-G-C

186320281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440846-G-T

186320384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22440936-T-C

http://identifiers.org/hco/3/GRCh38#186320635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22441118-C-A

186320635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22441118-C-G

186320635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22441118-C-T

186320644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22441127-T-G

186320674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22441154-G-A

186320674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22441154-G-T

http://identifiers.org/hco/3/GRCh38#186320729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22441208-A-C

186320729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22441208-A-T

186321123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22441618-A-G

186321202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22441692-G-C

186321459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22441934-T-C

http://identifiers.org/hco/3/GRCh38#186321610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22442050-A-C

186321646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442087-G-A

186321714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442185-A-G

186321721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442192-G-A

186321724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442195-G-A

186321993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442435-A-G

186322671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442625-A-G

http://identifiers.org/hco/3/GRCh38#186322777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22442720-C-A

186322777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442720-C-G

186322777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442720-C-T

186322945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442867-G-T

186322946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22442868-A-G

186323131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443029-T-C

186323185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443084-A-G

186323305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443192-C-T

186323306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443193-G-A

186323306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443193-G-T

186323485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443783-C-T

186323495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443791-T-C

186323527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443830-C-T

186323556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443857-G-C

186323621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22443913-G-C

186327977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449049-T-C

186328084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449136-T-G

186328198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449250-G-T

186329005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449671-C-T

186329130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449768-G-A

186329227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449864-C-T

186329309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22449946-C-T

186329433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22450068-G-A

http://identifiers.org/hco/3/GRCh38#186329636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22450264-A-C

186329918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22450741-C-G

186330522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22451358-C-T

186330572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22451418-C-T

http://identifiers.org/hco/3/GRCh38#186331300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22452116-C-A

186331616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452440-G-A

186331616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452440-G-C

186331616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452440-G-T

186331629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452453-G-T

186331657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452492-G-A

186331750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452552-G-A

186332130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452922-C-G

186332184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22452970-G-A

186332267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453047-T-C

186332314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453094-G-A

186332467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453120-G-A

186332480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453133-C-T

186332514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453151-C-G

186332638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453271-T-G

186332666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453302-G-A

186333177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453378-G-A

186333177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453378-G-T

http://identifiers.org/hco/3/GRCh38#186333210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22453411-C-A

186333210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453411-C-T

186333519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453701-A-G

186333612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453795-G-A

186333718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22453907-C-T

186333923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454099-G-A

186334016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454198-G-A

186334022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454204-G-T

186334335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454489-T-A

186334335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454489-T-C

http://identifiers.org/hco/3/GRCh38#186334501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22454650-A-C

http://identifiers.org/hco/3/GRCh38#186334519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22454665-C-A

186334629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454742-A-G

186334677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22454790-T-C

186334882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455211-C-T

186334889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455218-A-G

186334897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455226-A-G

186334927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455256-T-C

186334976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455305-G-A

186334976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455305-G-C

186335027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455340-C-G

186335797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22455838-A-G

186336041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22456183-G-A

186336291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22457431-A-G

186336433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22457568-C-G

186338839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22458353-T-C

186338864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22458373-A-G

186338952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22458459-G-A

186338981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22458483-A-G

186339002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22458504-G-A

http://identifiers.org/hco/3/GRCh38#186339004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22458506-A-C

186339161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22458672-G-A

186340149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460250-A-T

186340303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460412-T-C

186340371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460463-A-G

http://identifiers.org/hco/3/GRCh38#186340487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22460578-C-A

186340596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460690-T-G

186340666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460754-A-G

186340725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460793-A-G

186340725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460793-A-T

http://identifiers.org/hco/3/GRCh38#186340736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22460804-A-C

186340823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460867-A-G

186340875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22460916-A-G

186341054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22461066-C-T

186346347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462442-T-C

186346451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462544-A-T

186346474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462567-A-G

186346525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462595-G-A

186346525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462595-G-T

186346610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462677-A-G

186346622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462689-A-G

186346643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462708-T-G

186346721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462758-A-G

186346829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462866-G-A

186346932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462966-C-G

186346932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462966-C-T

186346944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462977-T-C

186346965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22462999-T-C

186346978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22463012-G-A

186353867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22467733-T-A

186354072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22467920-A-G

186354457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468280-A-G

186354523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468348-G-A

186354524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468349-G-T

186354530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468354-G-T

186354548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468372-A-G

186354551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468375-G-C

186354692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22468895-C-T

186354911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22469218-A-G

186354982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22469303-T-C

186355113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22469432-C-T

186355134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22469453-C-T

186355163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22469482-A-G

186355168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22469487-C-T

186357245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470426-A-G

186357281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470460-T-G

186357290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470469-T-C

186357352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470531-T-G

186357810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470881-T-C

186357894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470958-C-T

186357904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470968-G-A

186357929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470993-C-G

186357929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22470993-C-T

186358741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22472101-C-G

186358763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22472123-T-G

http://identifiers.org/hco/3/GRCh38#186359500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22472937-A-C

186359551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22472972-G-A

http://identifiers.org/hco/3/GRCh38#186359840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22473243-C-A

http://identifiers.org/hco/3/GRCh38#186360586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22474353-A-C

186360959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 22474730-G-T

http://identifiers.org/hco/3/GRCh38#186360960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#22474731-C-A

http://identifiers.org/hco/3/GRCh38#186361220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#22474993-C-A

186361334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22475124-C-G

186361851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22475611-G-A

186361851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22475611-G-T

186362160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5 prime UTR variant
orthologous variants: 22475881-G-A

186362160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5 prime UTR variant
orthologous variants: 22475881-G-C

186362160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2853
most severe consequence: 5 prime UTR variant
orthologous variants: 22475881-G-T