184812189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21241942-G-A

184812189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21241942-G-T

184812207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21241957-G-A

184812207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21241957-G-T

184812210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21241960-A-G

184812231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21241981-G-C

184812231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21241981-G-T

http://identifiers.org/hco/3/GRCh38#184812348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21242035-C-A

184812348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242035-C-T

184812391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242068-C-G

184812404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242083-C-T

http://identifiers.org/hco/3/GRCh38#184812453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21242107-C-A

184812453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21242107-C-T

184812751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21242195-G-A

184812751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21242195-G-T

184812885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242235-G-C

184812916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242266-T-C

184813067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242394-T-C

184813684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21242930-T-C

184815630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21244354-G-A

184815690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21244404-A-G

http://identifiers.org/hco/3/GRCh38#184816748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21244710-C-A

184816786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21244742-G-C

184816786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21244742-G-T

184816946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21244874-C-T

http://identifiers.org/hco/3/GRCh38#184817223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21245112-C-A

184817286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21245195-G-T

184817293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21245204-A-G

184817293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21245204-A-T

184817344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21245247-G-T

http://identifiers.org/hco/3/GRCh38#184817355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21245257-C-A

184817377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21245279-A-G

184817382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21245284-A-G

184817967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21245936-G-A

184821019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249067-T-C

184821094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249144-G-C

184821228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249300-G-C

184821240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249312-G-A

http://identifiers.org/hco/3/GRCh38#184822018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21249675-A-C

184822031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249688-G-A

184822046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249702-T-C

184822056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249712-A-G

184822146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21249799-A-G

184822569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21250373-A-G

184822928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21251414-A-G

184823711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21252666-G-A

184823824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21252945-G-C

184823825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21252946-A-G

184823885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253007-T-C

184824162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21253239-A-G

184824195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21253263-T-C

184824287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253351-T-A

184824329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253401-A-T

184824330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253402-G-T

184824353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253416-T-C

184824384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253447-C-T

http://identifiers.org/hco/3/GRCh38#184824396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21253459-C-A

184824396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253459-C-G

184824396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253459-C-T

184824447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253502-A-T

184824463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21253518-T-A

184824599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 21253627-T-C

184824600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 21253628-T-C

184824632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 21253660-T-C

184824652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21253680-A-G

184824708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21253736-T-C

http://identifiers.org/hco/3/GRCh38#184824713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21253741-C-A

184824713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21253741-C-G

184824713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21253741-C-T

184824747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21253775-A-G

184824771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21253799-T-A

184824782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21253810-T-C

184824800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21253828-T-G

184824873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21253888-T-C

184824904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21253919-A-T

http://identifiers.org/hco/3/GRCh38#184824927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21253953-A-C

184824927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21253953-A-G

184824927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21253953-A-T

http://identifiers.org/hco/3/GRCh38#184824929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21253955-A-C

184824929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 21253955-A-G

184824929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 21253955-A-T

184825968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254353-A-G

184826087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254435-T-G

http://identifiers.org/hco/3/GRCh38#184826103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21254451-C-A

184826103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254451-C-G

184826103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254451-C-T

184826284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254621-A-G

184826396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254919-T-C

184826441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254964-C-T

184826447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21254970-G-A

184826519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21255034-G-A

http://identifiers.org/hco/3/GRCh38#184828492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21257194-A-C

184828862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21257582-T-C

184829130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21257781-A-G

184829806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21258208-C-T

184829807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21258209-G-A

184829807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21258209-G-T

184830087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21258440-G-C

184830143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21258495-A-G

184830180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21258532-G-A

184830532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21259616-G-A

184830673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21259731-C-T

184831925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260370-G-T

184832020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260460-G-C

184832020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260460-G-T

184832163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260593-C-G

http://identifiers.org/hco/3/GRCh38#184832184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21260615-A-C

184832563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260950-A-T

184832567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260954-A-G

184832576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21260968-A-G

184832630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21261021-G-A

184832630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21261021-G-T

184832664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21261059-A-G

184832670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21261065-T-C

184832751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21261146-T-A

184832822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21261217-A-G

http://identifiers.org/hco/3/GRCh38#184832846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21261242-C-A

184833076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21261393-A-G

http://identifiers.org/hco/3/GRCh38#184833355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21261662-A-C

184834014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21262359-G-A

184834279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21262594-G-A

184834353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21262658-G-A

184834459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21262705-C-T

184834621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21262815-T-C

184834667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21262857-T-C

184834761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21262948-T-A

184834907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21263088-G-A

184834907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21263088-G-T

184834910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21263091-A-G

http://identifiers.org/hco/3/GRCh38#184834921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21263102-C-A

184834921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21263102-C-G

184834984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263164-T-C

184834987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263167-G-A

184834987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263167-G-T

184834998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263178-T-C

184835002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263182-A-G

http://identifiers.org/hco/3/GRCh38#184835047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21263218-C-A

184835047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263218-C-T

184835365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263341-G-T

http://identifiers.org/hco/3/GRCh38#184835439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21263410-A-C

184835515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21263474-T-G

http://identifiers.org/hco/3/GRCh38#184836098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21263698-C-A

184836592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21264187-A-T

184836718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21264308-T-A

184836911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21264465-C-T

184836923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21264477-T-G

184837238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265150-G-A

184838027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265347-C-G

184838141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265450-G-A

184838195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265499-A-G

184838198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265502-A-G

184838277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265583-G-C

184838306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265611-A-G

184838384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265686-A-G

184838403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265703-C-G

184838475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265774-C-T

184838599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265895-T-A

184838691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21265980-A-G

184838710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21266001-T-C

184838710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21266001-T-G

184838882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266155-G-A

184838882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266155-G-T

184839044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266274-G-A

184839044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266274-G-T

184839045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266275-G-A

184839045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266275-G-T

http://identifiers.org/hco/3/GRCh38#184839057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21266289-C-A

http://identifiers.org/hco/3/GRCh38#184839136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21266360-C-A

184839184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266405-T-A

184839254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266471-T-C

184839293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266509-C-G

184839339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266551-C-G

184839339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266551-C-T

184839350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266560-G-A

184839350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266560-G-T

184839398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266618-A-G

184839398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266618-A-T

184839481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266934-G-A

184839481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266934-G-T

http://identifiers.org/hco/3/GRCh38#184839484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21266937-A-C

184839484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266937-A-G

184839484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21266937-A-T

http://identifiers.org/hco/3/GRCh38#184839558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21267005-C-A

184839558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267005-C-T

184839563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267010-A-G

184839568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267013-A-G

184839569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267014-T-G

184839584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267028-A-G

184839595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267039-G-A

184839595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267039-G-T

http://identifiers.org/hco/3/GRCh38#184839618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21267062-C-A

184839618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267062-C-T

184839619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267063-A-G

184839631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267067-T-C

184839712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21267113-G-A

184839712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21267113-G-T

184839930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267328-G-A

184839931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267329-C-T

184839968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267372-A-G

184839970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267374-A-G

184840021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267423-T-G

184840063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267465-T-G

184840225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267599-G-T

http://identifiers.org/hco/3/GRCh38#184840453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21267787-C-A

184840453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21267787-C-T

184840801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21267832-C-G

184840969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21267975-T-C

184840999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268006-G-A

184840999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268006-G-T

184841021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268030-A-G

184841160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268171-C-T

184841172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268183-T-A

184841201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268213-T-C

184841493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268613-G-A

184841493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268613-G-T

184841925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21268979-C-T

184842047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269095-C-T

184842386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269251-C-T

184842656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269576-C-T

184842894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269778-A-G

184842939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269817-G-T

184842940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269818-G-T

184842972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269846-G-T

184843104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21269982-T-C

184843128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270010-A-G

184843207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270073-T-A

184843207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270073-T-C

184843307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270174-G-A

184843307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270174-G-C

184843307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270174-G-T

http://identifiers.org/hco/3/GRCh38#184843314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21270181-A-C

184843314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270181-A-G

184843331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270197-T-C

184843387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270244-G-A

184843387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270244-G-T

184843463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270333-A-G

184844003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21270822-T-G

http://identifiers.org/hco/3/GRCh38#184844087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21270891-C-A

184844923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21271780-C-T

184844952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21271799-A-G

184845055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21271874-T-G

184845189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21271976-G-A

184845449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21272210-C-G

184845449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21272210-C-T

184845828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21272275-G-C

184846077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21272488-T-G

184846181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21272578-C-T

http://identifiers.org/hco/3/GRCh38#184846199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21272595-A-C

184846585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21273101-C-T

184846753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21273271-T-C

184846810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21273311-T-C

184848407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21274836-C-T

184848408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21274837-C-T

184848492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21274928-A-T

184849283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275165-T-C

184849342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275229-G-A

184849342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275229-G-C

http://identifiers.org/hco/3/GRCh38#184849525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21275797-C-A

184849525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275797-C-T

184849586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275848-T-A

184849597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275859-T-G

184849637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275898-A-G

184849648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21275909-G-T

184849875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21276074-G-A

184850635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21276764-A-G

184851003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277112-A-G

184851234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277324-A-G

http://identifiers.org/hco/3/GRCh38#184851329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21277413-C-A

184851584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277567-C-G

184851638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277621-C-G

184851766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277660-A-G

184851878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277769-C-T

184852072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21277908-T-G

184852275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278284-G-C

http://identifiers.org/hco/3/GRCh38#184852325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21278333-A-C

184852337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278345-G-A

184852353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278360-T-A

184852353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278360-T-C

184852364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278371-G-A

184852364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278371-G-T

184852408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278405-A-G

184852450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278446-T-C

184852451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278447-A-T

184852960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278908-C-T

http://identifiers.org/hco/3/GRCh38#184853040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21278986-C-A

184853040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21278986-C-G

184853106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279246-A-G

http://identifiers.org/hco/3/GRCh38#184853107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21279247-A-C

184853232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279357-T-C

184853549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279616-G-A

184853588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279653-G-A

184853734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279777-G-A

184853846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279861-T-C

184853846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21279861-T-G

184853935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21279950-T-C

http://identifiers.org/hco/3/GRCh38#184854260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21280270-A-C

184854516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21280459-G-A

184854801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21280693-A-G

184855026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21281499-G-A

184855026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21281499-G-C

184855078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21281551-A-G

184855143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21281609-T-G

184855216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21281677-T-C

184855435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282070-A-G

184855480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282112-T-G

184855538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282168-A-G

184855648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282280-G-T

184855685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282317-T-A

184855685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282317-T-C

184855687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282319-T-G

http://identifiers.org/hco/3/GRCh38#184855695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21282327-C-A

184855695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282327-C-T

184855704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21282338-T-A

184855824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21282458-T-A

http://identifiers.org/hco/3/GRCh38#184855837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21282479-A-C

184859908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21285089-G-T

184860043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21285222-A-G

184860047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21285226-T-C

184861131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21287516-G-A

184861153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21287553-G-T

184861160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21287560-A-G

184862731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21288731-T-G

http://identifiers.org/hco/3/GRCh38#184862757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21288756-C-A

184862757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21288756-C-G

184862797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21288784-T-A

http://identifiers.org/hco/3/GRCh38#184862799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21288786-C-A

184862911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21288881-C-T

184862965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21288935-A-G

184862995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21288965-A-G

184863245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289208-A-G

184863324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289487-A-G

184863339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289502-C-T

184863607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289740-C-T

http://identifiers.org/hco/3/GRCh38#184863610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21289743-A-C

184863630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289756-A-T

184863674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289797-G-A

184863749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289866-T-G

184863809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289931-A-G

184863812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21289934-G-T

184866861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21293983-A-G

184866861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21293983-A-T

184866961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294083-T-C

184867018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294130-T-A

184867018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294130-T-C

184867020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294132-G-A

184867076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294182-T-A

184867083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294189-T-G

184867090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294196-G-A

184867090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21294196-G-T

http://identifiers.org/hco/3/GRCh38#184867959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21295166-A-C

184868223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21295400-G-A

184868278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21295587-G-A

184868278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21295587-G-T

184868283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21295592-A-T

184868290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21295599-T-C

184868320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295629-A-G

184868323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21295632-T-C

184868727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21296016-A-G

http://identifiers.org/hco/3/GRCh38#184868852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21296151-C-A

184868914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21296205-G-T

184868915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21296206-G-T

184868920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21296211-T-C

184868981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21296271-A-G

184869044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21296334-G-A

http://identifiers.org/hco/3/GRCh38#184869133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21296363-C-A

184869133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296363-C-G

184869133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296363-C-T

184869134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296364-G-A

184869134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296364-G-T

http://identifiers.org/hco/3/GRCh38#184869135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21296365-A-C

184869135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296365-A-G

184869270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296396-A-G

184869376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296490-A-G

184869435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296550-G-A

184869435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296550-G-T

184869510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21296623-G-A

184870413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21296874-T-G

184870608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297035-A-G

184870608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297035-A-T

http://identifiers.org/hco/3/GRCh38#184870609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21297036-A-C

184870609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297036-A-G

184870609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297036-A-T

184870624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297056-T-A

184870624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297056-T-C

184870624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297056-T-G

184870625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297057-T-A

184870625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297057-T-C

184870625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297057-T-G

184870645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297077-G-A

184870645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297077-G-T

184870661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297089-T-A

184870661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297089-T-C

184870692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21297120-T-C

184870766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21297194-A-G

http://identifiers.org/hco/3/GRCh38#184870816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21297245-C-A

184870816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297245-C-T

http://identifiers.org/hco/3/GRCh38#184870838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21297273-C-A

184870838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297273-C-G

184870838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297273-C-T

184870881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297325-G-A

http://identifiers.org/hco/3/GRCh38#184870949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21297385-C-A

184870979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21297412-T-C

184871732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21301474-A-T

184871764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21301494-T-C

184875050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21305403-T-A

184875078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21305438-G-C

184875078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21305438-G-T

184875241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21307350-G-C

184875278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21307362-C-T

184885935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21314461-G-A

184885935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21314461-G-T

184885976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314500-A-G

184885976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314500-A-T

184886015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314539-T-C

184886056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314581-T-C

184886058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314583-G-A

184886058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314583-G-T

184886062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21314587-A-G

184886114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 21314634-T-C

184886151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21314671-G-A

184886171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21314691-C-T

184886175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21314695-T-G

184886912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315145-C-T

184887394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315306-C-G

184887485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315369-G-A

184887518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315394-A-G

184887592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315461-C-G

184887791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315654-G-T

184887792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315655-G-T

184888539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21315919-A-G

184888717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316075-A-G

184888856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316161-A-G

184888905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316189-G-C

184889033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316311-C-G

184889034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316312-C-G

184889153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316473-G-A

184889199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316517-A-G

184889265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316561-A-G

http://identifiers.org/hco/3/GRCh38#184889544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21316755-C-A

184889751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21316945-T-G

184889793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21316988-A-G

184889886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317074-T-A

184889969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317133-C-G

184889991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317155-G-A

184890042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317204-A-G

184890075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317233-A-G

184890075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317233-A-T

184892068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21317909-C-T

184892552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318049-T-G

184892556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318053-G-A

184892557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318054-C-G

184892732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318207-A-T

184894560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318798-A-G

184894574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318814-A-G

184894578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318818-T-C

184894632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318870-A-G

184894653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21318888-G-A

184894739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21318974-T-G

184894751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21318986-G-A

http://identifiers.org/hco/3/GRCh38#184895013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21319226-C-A

184895013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319226-C-T

184895132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319314-A-T

184895201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319376-A-G

184895243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319409-C-G

184895252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319418-C-T

184895253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319419-G-A

184896047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319845-A-T

184896145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319926-C-T

184896223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21319994-T-C

184896418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21320162-A-G

184896453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21320190-C-G

184896453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21320190-C-T

184896467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21320199-T-C

184896653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21320393-T-G

http://identifiers.org/hco/3/GRCh38#184896736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21320473-A-C

http://identifiers.org/hco/3/GRCh38#184896924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21320771-C-A

184898106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21322737-C-T

184898168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21322791-C-G

184898204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21322823-A-G

184898204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21322823-A-T

184898271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21322863-T-C

184898394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21322990-A-G

184898419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323010-G-A

184898419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323010-G-T

184898445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323035-A-G

184898445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323035-A-T

184898467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323060-T-A

184898467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323060-T-C

184898467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323060-T-G

http://identifiers.org/hco/3/GRCh38#184898486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21323075-A-C

184898545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323129-G-A

184898600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21323183-T-C

184898673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323256-T-C

http://identifiers.org/hco/3/GRCh38#184898679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21323261-C-A

184898679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323261-C-T

184898680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323262-G-A

184898680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323262-G-T

http://identifiers.org/hco/3/GRCh38#184898725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21323297-C-A

184898725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323297-C-T

http://identifiers.org/hco/3/GRCh38#184898730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21323302-A-C

184898732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323304-T-C

184898732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323304-T-G

184898733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323305-A-G

184898741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323311-G-T

184898751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323321-A-G

184898751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21323321-A-T

184900833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21325435-G-A

184900833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21325435-G-T

http://identifiers.org/hco/3/GRCh38#184912724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21329621-A-C

184912724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21329621-A-G

184912767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21329652-A-T

184912898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21329764-A-G

184913243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330044-G-T

184913379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330148-G-T

184913395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330164-T-C

http://identifiers.org/hco/3/GRCh38#184913419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21330188-C-A

184913429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330198-A-G

184913506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330256-C-G

184913506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330256-C-T

184913604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330352-A-G

184913606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330354-A-G

http://identifiers.org/hco/3/GRCh38#184913613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21330375-C-A

184913613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330375-C-G

184913613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330375-C-T

184913614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330376-T-C

184913631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330429-T-A

184913632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330430-A-G

184913632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330430-A-T

184913661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330495-T-C

184913671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330505-T-C

184913691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330569-G-A

184913691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330569-G-T

184913692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330570-T-C

184913703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330581-G-T

184913708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330586-A-G

http://identifiers.org/hco/3/GRCh38#184913731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21330606-A-C

184913731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330606-A-T

184913850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330775-T-C

184913851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21330776-A-G

http://identifiers.org/hco/3/GRCh38#184914201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21331098-C-A

184914201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21331098-C-G

184914366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21331261-C-T

184914378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21331273-G-A

184914486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21331382-C-G

184914604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21331487-C-G

184914881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21335969-A-G

184914886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21335974-G-T

184914904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21335992-T-G

184915166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21336513-G-A

184915247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21336606-T-C

184915282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21336641-A-G

184915282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21336641-A-T

184915387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21336895-A-G

184915387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21336895-A-T

184915399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21336907-T-C

184916125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337257-G-A

184916165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337297-G-A

184916187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337317-A-G

184916301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337432-G-A

184916301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337432-G-T

184916368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337503-G-A

184916513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337643-T-C

http://identifiers.org/hco/3/GRCh38#184916608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21337731-C-A

184916648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21337771-G-A

184918251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21338148-C-T

184918460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21338260-T-C

184918804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21338580-T-C

184918892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21338663-G-A

184919240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21339046-A-G

184920193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21340700-T-C

http://identifiers.org/hco/3/GRCh38#184920282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21340790-C-A

184920283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21340791-T-A

184920283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21340791-T-C

184920403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21340895-C-G

184920427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21340921-A-G

184920724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21341191-G-A

184920905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21341338-G-A

184921072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21341505-C-G

184921152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21341577-T-C

184921169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21341595-A-G

184921335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21341746-C-T

184922096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21342693-G-A

http://identifiers.org/hco/3/GRCh38#184922183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21342765-C-A

184922307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21342846-A-G

184922422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21342990-G-T

184922431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21342999-T-A

184922536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21343108-T-A

184922545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21343117-T-A

184922577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21343161-T-C

184922633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21343201-A-G

184922733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21343282-A-G

184923256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21343930-A-G

184923413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21344067-C-G

http://identifiers.org/hco/3/GRCh38#184923431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21344082-C-A

184923445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21344096-C-T

184923828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21344376-T-C

184924789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345044-T-A

184924789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345044-T-C

184925020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345287-G-C

http://identifiers.org/hco/3/GRCh38#184925100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21345324-C-A

184925100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345324-C-G

184925100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345324-C-T

184925171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345405-G-A

184925179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345412-A-G

184925592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21345989-G-A

184925606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21346003-G-C

184926617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21346309-T-C

184926625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21346317-A-T

184926627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21346319-T-C

http://identifiers.org/hco/3/GRCh38#184926676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21346365-C-A

184926676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346365-C-T

184926756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346398-G-T

184927089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346598-C-G

184927293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346788-T-A

184927398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346847-G-A

184927398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346847-G-T

184927479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21346921-T-C

184927715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21349050-A-G

184927825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21349167-C-T

184927842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21349185-C-T

184927959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21349352-A-G

http://identifiers.org/hco/3/GRCh38#184928377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21349947-C-A

184928630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350200-T-C

184928962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350633-C-T

184929029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350694-C-G

184929094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350735-C-T

184929105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350746-A-G

184929164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350794-A-G

184929431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350888-C-G

184929478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350931-G-T

184929491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350949-A-G

184929533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21350987-A-G

184929610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21351063-A-G

184929610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21351063-A-T

184929649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21351102-T-A

184929655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21351108-T-C

184929702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351155-A-T

184929713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351166-T-C

184929713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351166-T-G

184929718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351171-G-A

184929718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351171-G-T

184930085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351442-A-G

184930131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351487-G-T

184930414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351754-A-G

184930416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351756-G-T

184930426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351770-T-C

184930429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351773-A-T

184930444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21351788-A-G

184930553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21351896-A-G

184931542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21353266-G-A

184931542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21353266-G-C

184931848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21353516-G-T

184932017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21353670-G-A

184935691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358259-A-G

184935795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358356-A-T

184936219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358744-T-A

184936219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358744-T-C

184936221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358746-G-A

184936221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358746-G-T

http://identifiers.org/hco/3/GRCh38#184936282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21358805-C-A

184936282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21358805-C-G

http://identifiers.org/hco/3/GRCh38#184936320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21358843-C-A

184936351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358874-A-G

184936413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358910-A-G

184936489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21358976-A-G

184936562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359085-G-T

184936612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359135-T-C

184936728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359247-C-G

184937186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359407-T-A

184937514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359596-C-G

184937695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359750-G-T

184937763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359807-A-G

184937930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359955-A-G

184938002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21360020-A-G

184938557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21360601-G-T

184938623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21360664-A-G

184938626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21360667-A-T

184938710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21360718-G-T

184939323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21361263-T-A

184939353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21361296-C-G

184939892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21361795-A-T

184939893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21361796-C-G

184940202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21362023-G-A

184940202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21362023-G-T

184940263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362083-T-A

184940263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362083-T-C

184940320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362135-A-G

184940368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362184-G-A

184940401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362212-T-C

184940406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362217-G-T

184940828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362625-G-T

184940902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362698-G-T

184940919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362715-A-G

184940919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362715-A-T

http://identifiers.org/hco/3/GRCh38#184944412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21366450-C-A

184944412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366450-C-G

184944412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366450-C-T

184944426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366462-T-A

184944469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366500-T-C

184944487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21366517-C-T

184944623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366624-G-T

184944817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366807-T-G

184945134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21367098-C-G

184945134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21367098-C-T

http://identifiers.org/hco/3/GRCh38#184945145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21367109-C-A

http://identifiers.org/hco/3/GRCh38#184945169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21367133-C-A

184945293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21367377-A-G

184946501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21367843-G-A

184946674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21367994-T-G

184946729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21368050-T-G

184946772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21368093-C-G

184957032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21372561-A-G

184957101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21372626-A-G

184957285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21372749-G-T

184957341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21372792-A-G

184957341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21372792-A-T

184957385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21372836-A-G

184957441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21372892-C-T

184957555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21373004-A-G

184961351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21373631-C-T

184961536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21373940-A-G

184961611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374024-A-T

http://identifiers.org/hco/3/GRCh38#184961720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21374114-C-A

184962318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374471-A-G

184962363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374507-A-G

184962461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374600-C-G

184962515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374651-C-T

184962588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374723-G-A

184962911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374990-A-G

184962999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376284-A-G

184963168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376445-C-T

184963359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376598-G-A

184963572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376857-A-G

184963836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21377194-G-T

http://identifiers.org/hco/3/GRCh38#184964186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21377837-A-C

184964186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21377837-A-G

184964219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21377866-A-G

184964322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21377958-G-T

184964453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378069-T-C

184964453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378069-T-G

http://identifiers.org/hco/3/GRCh38#184964485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21378101-A-C

184964485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21378101-A-G

184964530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21378146-T-A

184964530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21378146-T-C

184966598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378883-G-A

184966607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378892-A-G

184966607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378892-A-T

184966610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378895-A-G

184966619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378904-G-A

184966619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378904-G-C

184966619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378904-G-T

184966634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378919-G-A

184966647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378929-T-A

184966647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378929-T-C

184966708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21378985-G-A

184966716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378993-A-G

184966841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21379081-T-A

184968697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380170-T-C

184968756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380225-T-G

184968826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380296-C-T

184968962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380424-T-C

184969011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380463-C-T

184969082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380537-G-A

184969087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380542-A-G

http://identifiers.org/hco/3/GRCh38#184970332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21380809-C-A

184970332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380809-C-T

184970391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21380863-G-A

184970566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381019-A-T

184970598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381046-G-A

184970806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381158-T-C

184970834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381185-T-C

184971078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381378-G-C

184971564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381800-G-T

184971601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381834-T-G

184971622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21381853-T-C

184971772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382006-G-C

184972133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382058-T-C

184972212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382137-G-A

184972337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382271-G-T

184972385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382319-C-T

http://identifiers.org/hco/3/GRCh38#184972506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21382442-A-C

184972658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382573-C-G

184972687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382599-A-G

184972812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382718-A-G

184972854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382766-C-T

184972869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382781-T-C

184972988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21382911-G-A

184973227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383372-A-G

184982024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21386395-C-T

http://identifiers.org/hco/3/GRCh38#184982050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21386421-C-A

184982260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21386555-T-C

http://identifiers.org/hco/3/GRCh38#184982430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21386655-C-A

184982430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21386655-C-G

184982430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21386655-C-T

184982561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21386714-T-C

184982622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21386775-A-G

184982623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21386776-G-A

184982623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21386776-G-C

184982623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21386776-G-T

http://identifiers.org/hco/3/GRCh38#184982659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21386815-A-C

184982684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21386838-G-A

184982684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21386838-G-C

http://identifiers.org/hco/3/GRCh38#184982911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21387062-C-A

184982911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387062-C-T

184983040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21387167-A-G

http://identifiers.org/hco/3/GRCh38#184983064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21387191-C-A

184983064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21387191-C-T

184983107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387234-G-A

184983107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387234-G-C

184983107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387234-G-T

184983125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387248-G-C

184983125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387248-G-T

184983140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387255-T-A

184983140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387255-T-G

184983147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387262-A-G

184983148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387263-T-A

184983148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387263-T-C

184983166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387276-T-A

184983223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387316-A-G

184983351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387388-C-G

184983351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387388-C-T

184983622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387685-C-T

184983662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387726-A-G

http://identifiers.org/hco/3/GRCh38#184983815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21387874-A-C

184983825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387884-A-G

184983826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387885-T-G

184983875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387915-G-T

184984319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388165-G-A

184984319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388165-G-T

184984328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388173-T-C

184984453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388257-C-T

184984626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388293-T-A

184984793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388437-T-A

184984804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388448-T-G

184984845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388488-T-C

184985094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21388707-C-T

184990719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21389873-T-C

184990783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21389935-G-A

184990886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390034-G-A

184990886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390034-G-C

184990886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390034-G-T

184991026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390587-T-G

184991092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390649-C-T

184991365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390886-G-A

184991434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390953-T-G

184991542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391064-C-T

184991682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391205-T-C

184991960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391440-G-A

184992016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391489-G-A

184992017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391490-G-T

184992156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391627-A-G

184992259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391711-G-C

http://identifiers.org/hco/3/GRCh38#184992490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21392080-A-C

184992566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392304-G-C

184992643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392417-A-G

184992712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392479-T-A

184992796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392557-C-T

184992865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392626-A-G

184992890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392651-C-G

184992915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392676-G-T

184993038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392780-A-G

184993038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392780-A-T

http://identifiers.org/hco/3/GRCh38#184993220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21392902-A-C

184993225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392907-T-C

184993299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392948-C-T

184993347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392968-G-T

184993376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392985-A-T

184993397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393005-G-T

184993609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393200-T-A

184993609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393200-T-C

http://identifiers.org/hco/3/GRCh38#184993632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21393222-C-A

http://identifiers.org/hco/3/GRCh38#184993642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21393232-C-A

184993662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393252-A-G

http://identifiers.org/hco/3/GRCh38#184993709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21393291-A-C

184993728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393296-A-G

184993885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393444-A-G

184993937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393665-T-A

184994102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393835-G-A

184994111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393850-T-C

http://identifiers.org/hco/3/GRCh38#184994139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21393883-C-A

184994183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393933-G-A

184994183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21393933-G-T

184994198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394007-G-C

184994198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394007-G-T

184994200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394009-A-G

http://identifiers.org/hco/3/GRCh38#184994240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21394134-A-C

http://identifiers.org/hco/3/GRCh38#184994254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21394148-C-A

184994277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394170-G-A

http://identifiers.org/hco/3/GRCh38#184994684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21394288-A-C

184994764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394350-A-G

184995637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394768-A-G

http://identifiers.org/hco/3/GRCh38#184995639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21394770-C-A

184995878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21394993-A-T

http://identifiers.org/hco/3/GRCh38#184996043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21395153-A-C

184996165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395271-G-C

184996211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395294-G-A

184996211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395294-G-T

184996226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395309-C-T

184996531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395573-T-C

184996588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395624-T-C

184996592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395628-T-G

184996644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395680-G-A

184996644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395680-G-T

184996818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395871-G-A

184996924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395969-G-A

184996924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395969-G-T

184996944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395989-A-G

184997060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396095-G-A

184997159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396196-G-A

184997258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396305-C-T

184998883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21399976-C-T

184999498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400094-C-T

184999548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400142-A-G

http://identifiers.org/hco/3/GRCh38#184999577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21400172-C-A

184999577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400172-C-T

184999683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400270-C-G

184999692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21400279-G-A

184999692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21400279-G-T

184999744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21400331-T-C

http://identifiers.org/hco/3/GRCh38#184999765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21400352-A-C

184999850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21400437-A-G

184999877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400464-G-A

184999877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400464-G-C

184999878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400465-T-A

184999878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400465-T-C

184999878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400465-T-G

http://identifiers.org/hco/3/GRCh38#184999933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21400491-C-A

184999933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400491-C-T

184999978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400533-G-A

184999978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400533-G-T

http://identifiers.org/hco/3/GRCh38#185000008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21400554-A-C

185000008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400554-A-G

185000015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400559-G-A

185000189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400704-G-T

185000300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21400846-G-T

185000460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401008-C-T

185006916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408522-A-G

185006977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408571-C-T

http://identifiers.org/hco/3/GRCh38#185007094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21408697-A-C

185007390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408967-A-G

185007889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409937-T-G

185007920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21409970-A-T

185008028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410061-A-G

185008188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410209-A-G

185008329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410310-G-A

185021349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414458-C-T

http://identifiers.org/hco/3/GRCh38#185024352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#21426934-C-A

185024352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21426934-C-T

http://identifiers.org/hco/3/GRCh38#185024467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21427046-A-C

185024467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427046-A-T

185024533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427107-T-C

185024642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427219-G-A

185024642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427219-G-C

185025213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427416-C-T

185025268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21427469-G-A

185025753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21428282-G-T

185028102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21429632-G-A

185028722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430201-C-T

http://identifiers.org/hco/3/GRCh38#185028793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21430233-C-A

185028793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430233-C-G

185029200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430578-C-T

185029627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21430872-T-C

185030098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431124-G-T

185030215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21431185-A-G

185031143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432002-G-T

185031149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432008-G-C

185031489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432086-A-G

185031668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21432236-G-T

185042540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444533-C-G

185042678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444634-C-G

185042742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21444695-T-C

185043127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445242-G-A

185043548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445634-C-T

185043549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445635-G-A

185043551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445637-G-A

185043642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445699-T-C

185043765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445780-G-T

185044231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445889-A-T

185044248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21445906-G-A

185044718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446258-T-C

185044944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446456-G-A

185044944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446456-G-T

185045045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446550-G-A

185045071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446579-A-G

185045245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446741-A-G

185045375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21446835-C-T

185046090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21447205-G-A

185046253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449534-G-C

185046287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449576-T-A

185046308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449607-C-T

http://identifiers.org/hco/3/GRCh38#185046330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21449629-C-A

185046482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449773-G-T

185046731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21449992-G-A

185046866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450115-G-A

185046949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450189-G-T

185047236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450456-T-C

185047317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450515-A-G

185047387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450572-G-A

185047390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21450575-C-G

185048337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459281-A-G

185048337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459281-A-T

185048346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459290-T-A

185048346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459290-T-C

185048346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459290-T-G

185048367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459308-G-A

185048367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459308-G-T

185048374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459315-G-A

185048374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459315-G-T

185048382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459323-A-G

185048394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459338-T-G

185048427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459368-G-A

185048538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21459488-T-C

http://identifiers.org/hco/3/GRCh38#185048595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21459535-C-A

185048595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459535-C-G

185048595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459535-C-T

185049036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21459970-C-T

185049492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460569-G-A

185049493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460570-G-A

185049514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460590-C-T

185049716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460733-C-T

185049759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460758-G-C

185049776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460775-C-G

185050037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460984-G-A

185050037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21460984-G-T

185050145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461074-A-G

185050145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461074-A-T

185050565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461910-A-G

185050576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461918-C-G

185050576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461918-C-T

185050577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461919-G-A

185050577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461919-G-T

185050584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461926-T-C

185050593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461939-G-A

185050646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21461989-A-G

185050834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462183-C-T

185051345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462560-G-A

185051729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462761-T-G

http://identifiers.org/hco/3/GRCh38#185051820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21462803-C-A

185051820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462803-C-G

185051820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462803-C-T

185051822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462805-T-C

185051867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21462862-C-T

http://identifiers.org/hco/3/GRCh38#185051893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21462888-A-C

185051941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21462936-G-A

185051941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21462936-G-C

185051941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21462936-G-T

185051966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21462961-A-G

185051966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21462961-A-T

185052001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21462996-T-A

http://identifiers.org/hco/3/GRCh38#185052087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21463063-C-A

185052087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463063-C-T

185052098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463069-T-A

http://identifiers.org/hco/3/GRCh38#185052159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21463118-C-A

185052159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463118-C-T

185052171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463129-A-G

185052171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463129-A-T

185052174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463132-G-A

185052174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463132-G-T

http://identifiers.org/hco/3/GRCh38#185052176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21463134-A-C

185052176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463134-A-T

http://identifiers.org/hco/3/GRCh38#185052178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21463136-C-A

185052178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463136-C-T

http://identifiers.org/hco/3/GRCh38#185052182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21463140-C-A

185052182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463140-C-G

185052182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463140-C-T

185052255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463199-G-A

185052255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463199-G-T

185052273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463207-T-C

185052273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463207-T-G

http://identifiers.org/hco/3/GRCh38#185052351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#21463262-A-C

185052351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463262-A-G

185052507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463332-T-C

185052507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29122
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21463332-T-G