120013093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119576662-A-T

120013165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119576587-G-A

120013165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119576587-G-T

120013195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119576535-G-A

120013262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119576474-G-A

120013262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119576474-G-T

120013271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119576465-A-G

120013485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119576318-G-C

http://identifiers.org/hco/2/GRCh38#120013501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#119576299-C-A

120013501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119576299-C-G

120013596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119576243-A-G

120014476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119574603-G-A

120014476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119574603-G-C

120016879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119571596-A-T

120016896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119571583-T-C

120016989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119571507-G-A

120016989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119571507-G-T

120017049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119571442-G-A

120017154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119571327-T-G

120017347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119571177-G-A

120017393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119571140-T-C

120019026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119570425-G-A

http://identifiers.org/hco/2/GRCh38#120019073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119570396-A-C

120019073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119570396-A-G

120019181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119570288-A-T

120019278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119570191-G-A

120019301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119570168-G-A

120019301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119570168-G-T

http://identifiers.org/hco/2/GRCh38#120019306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119570163-C-A

120019306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119570163-C-T

http://identifiers.org/hco/2/GRCh38#120019393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119570110-C-A

120019393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119570110-C-T

http://identifiers.org/hco/2/GRCh38#120020348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119569508-A-C

120020348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119569508-A-G

120020503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119569314-G-A

http://identifiers.org/hco/2/GRCh38#120026702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119568349-A-C

120026773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119568280-G-A

120027239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119567751-G-A

120027560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119567242-A-G

120027578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119567224-T-C

120027578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119567224-T-G

120027591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119567203-G-A

120027592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119567202-A-G

120027873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119566960-T-A

http://identifiers.org/hco/2/GRCh38#120028607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119566626-A-C

120029010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119566306-G-A

120029127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119566231-G-A

120032747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119564424-G-A

120034158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119564128-G-A

120034358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119563945-C-G

http://identifiers.org/hco/2/GRCh38#120035826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119563121-A-C

120035826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119563121-A-G

120041960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561421-A-G

120042144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119561243-G-A

120042608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119560713-T-G

120045438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558852-A-G

http://identifiers.org/hco/2/GRCh38#120045511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119558786-A-C

120045511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558786-A-G

120045635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119558677-C-T

120064525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119555129-T-C

120064646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119555011-T-C

120064897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119554752-A-G

120067121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119552799-T-C

120067271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119552566-A-G

120067438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119552389-T-A

120067438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119552389-T-C

120067584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119552258-T-G

120067684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119552110-G-A

120067845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119551928-G-A

http://identifiers.org/hco/2/GRCh38#120073133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119551745-A-C

120073133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119551745-A-G

http://identifiers.org/hco/2/GRCh38#120073327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119551546-C-A

120073949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549840-A-G

120073954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549835-A-T

120074089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549703-T-C

http://identifiers.org/hco/2/GRCh38#120074192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119549608-C-A

120074192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549608-C-G

120074192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549608-C-T

120074207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549593-G-T

120074224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549557-T-A

120074239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549542-A-G

120074239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549542-A-T

http://identifiers.org/hco/2/GRCh38#120074271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119549517-A-C

120074271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549517-A-G

120074315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549502-T-G

http://identifiers.org/hco/2/GRCh38#120074342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119549472-A-C

120074342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119549472-A-G

http://identifiers.org/hco/2/GRCh38#120074360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119549452-C-A

120074409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549421-G-C

120074409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549421-G-T

120074510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549316-T-A

120074510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549316-T-C

120074594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549242-T-C

120074653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549185-A-G

120074790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119549030-A-G

120074831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119548980-A-G

120074986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119548892-C-T

120074998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119548880-T-A

120075767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547881-A-T

120075836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547814-G-A

120075836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547814-G-T

120075845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547805-A-G

120075862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547788-T-C

120075874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547778-G-A

120075874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119547778-G-T

120076919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119545461-T-C

120077036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119545337-C-G

120077036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119545337-C-T

120077096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119545277-C-T

120077157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119545224-C-T

120077213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119545195-T-C

120077466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119544713-T-A

120077466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119544713-T-C

http://identifiers.org/hco/2/GRCh38#120077468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119544711-C-A

120078706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119544024-T-A

120078766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543967-T-C

120078829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543906-A-G

120086754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543514-G-T

120087028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543247-G-A

120087028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543247-G-T

120087072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543211-G-A

120087072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119543211-G-T

120087374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119542964-A-G

120090279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119537070-T-C

120090594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119536798-A-G

120090614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119536779-A-G

120091160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119536307-A-T

120091228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119536163-T-C

120091488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119535886-G-A

120091488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119535886-G-C

120091676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119535700-T-C

http://identifiers.org/hco/2/GRCh38#120091790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119535583-C-A

120091959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119535438-A-G

120093252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119532980-G-A

120093496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119532753-C-T

120096131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119531444-C-G

120096131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119531444-C-T

120096851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119531039-T-C

120097000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119530915-A-G

120097097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119530808-T-C

120097616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119530105-A-G

http://identifiers.org/hco/2/GRCh38#120097890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119529714-C-A

120100210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119528000-A-G

120100210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119528000-A-T

120100260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119527952-T-G

120100261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119527951-C-T

http://identifiers.org/hco/2/GRCh38#120100320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119527892-C-A

120100568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119527680-G-A

120100568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119527680-G-T

http://identifiers.org/hco/2/GRCh38#120100649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119526894-A-C

http://identifiers.org/hco/2/GRCh38#120100662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119526881-A-C

120100712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526835-G-C

120100726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526821-G-A

120100747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526800-G-A

120100747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526800-G-C

120100748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526799-C-T

120100755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119526792-G-A

120100762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526785-G-C

120100795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526752-G-C

120100795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119526752-G-T

120101002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119526552-C-T

120101409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119526387-T-A

http://identifiers.org/hco/2/GRCh38#120101488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119526308-C-A

120101641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119526176-G-A

120101772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119526050-C-G

120101772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119526050-C-T

120101912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119525904-T-C

120101912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119525904-T-G

120102259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119525417-T-A

120102259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119525417-T-G

http://identifiers.org/hco/2/GRCh38#120102494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119525191-A-C

http://identifiers.org/hco/2/GRCh38#120102762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119524952-A-C

120102777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119524937-T-C

http://identifiers.org/hco/2/GRCh38#120103248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119524540-C-A

120103607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119524184-G-T

http://identifiers.org/hco/2/GRCh38#120103979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119523852-C-A

120103979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119523852-C-T

120103999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119523842-A-G

http://identifiers.org/hco/2/GRCh38#120104077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119523770-A-C

120104136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523711-G-A

120104136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523711-G-T

http://identifiers.org/hco/2/GRCh38#120104258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119523588-C-A

120104258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523588-C-T

120104262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523584-G-A

120104262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523584-G-T

120104355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523487-T-A

http://identifiers.org/hco/2/GRCh38#120104535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119523307-C-A

120104535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523307-C-G

120104535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523307-C-T

http://identifiers.org/hco/2/GRCh38#120104568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119523278-C-A

120104846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523023-A-G

120104865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119523004-G-A

120105073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119522839-G-T

120105118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119522795-T-A

120105401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119522559-T-C

120105622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119522375-A-G

120105720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119522266-G-A

120105858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119521894-C-G

120106053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119521700-T-C

120106153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119521600-G-T

120106488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119521032-T-C

120106849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119520218-G-A

120106849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119520218-G-T

120107455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119518725-T-G

120107538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119518644-G-A

120107838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119518436-C-G

120107838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119518436-C-T

http://identifiers.org/hco/2/GRCh38#120127695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119506798-C-A

120127695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119506798-C-G

120127803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119506690-G-A

120127904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119506402-A-G

http://identifiers.org/hco/2/GRCh38#120127928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119506378-C-A

120128004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119506316-G-A

120128004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119506316-G-C

120128004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119506316-G-T

http://identifiers.org/hco/2/GRCh38#120128232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119505988-A-C

120128295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119505954-T-G

120128309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119505940-G-A

120129583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119504134-C-G

120129631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119504089-A-G

120131733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500516-G-C

120131764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500490-C-T

120131765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500489-A-G

120131808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500443-G-C

120131808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500443-G-T

120131867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500042-A-G

120131900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119500009-T-C

http://identifiers.org/hco/2/GRCh38#120142969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119497929-A-C

120142969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119497929-A-G

120143120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense variant
orthologous variants: 119497784-G-A

http://identifiers.org/hco/2/GRCh38#120146071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119495732-A-C

120146099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119495716-A-G

http://identifiers.org/hco/2/GRCh38#120146138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119495676-C-A

http://identifiers.org/hco/2/GRCh38#120146280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119495533-C-A

120146280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense variant
orthologous variants: 119495533-C-T

120146327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119495486-T-C

120146337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119495474-T-C

120146388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron variant
orthologous variants: 119495424-T-C

120160899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119482852-T-A

http://identifiers.org/hco/2/GRCh38#120160906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119482845-C-A

120160969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119482785-C-G

http://identifiers.org/hco/2/GRCh38#120161006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119482755-C-A

120161006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482755-C-T

http://identifiers.org/hco/2/GRCh38#120161033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119482729-C-A

120161033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482729-C-G

120161033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482729-C-T

http://identifiers.org/hco/2/GRCh38#120161041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119482721-C-A

120161041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482721-C-T

120161056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482706-G-T

120164694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482142-G-T

120164768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482068-T-C

120164785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482053-A-G

120164794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482051-T-C

120164794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119482051-T-G

120164875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119481969-A-T

120164890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119481954-G-A

120164917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119481927-A-G

http://identifiers.org/hco/2/GRCh38#120164970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119481877-C-A

120164970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119481877-C-T

120164973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119481874-G-C

120164973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119481874-G-T

120165027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119481567-T-A

120165027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119481567-T-G

120167160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478531-T-A

120167260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478453-T-C

120167355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478389-A-T

120167357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478387-G-T

http://identifiers.org/hco/2/GRCh38#120167410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119478340-A-C

120167410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478340-A-G

120167452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478305-T-C

120167542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119478215-T-C

http://identifiers.org/hco/2/GRCh38#120168087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119477541-C-A

120168087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119477541-C-T

120168181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119477444-A-G

120168342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119477283-A-G

120168368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119477259-G-C

120168369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119477258-G-T

http://identifiers.org/hco/2/GRCh38#120174745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119476991-A-C

120174756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119476984-G-T

120174835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 119476929-T-C

120175032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119476752-T-G

120175057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119476727-T-G

http://identifiers.org/hco/2/GRCh38#120175126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119476667-A-C

120175201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476599-T-C

120175204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119476596-G-T

120175362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476447-G-T

http://identifiers.org/hco/2/GRCh38#120175403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119476408-C-A

120175410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476401-A-T

120175456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476364-A-T

120175473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476347-A-G

120175588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476248-G-A

120175588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119476248-G-T

120175745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119476104-G-T

http://identifiers.org/hco/2/GRCh38#120175837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119476033-A-C

120175967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475927-C-T

120176065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475848-A-G

120176066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475847-T-A

120176090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475823-C-T

120176213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475709-A-G

120176215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475707-G-A

http://identifiers.org/hco/2/GRCh38#120176659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119475316-C-A

120176765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475220-G-A

http://identifiers.org/hco/2/GRCh38#120176786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119475203-C-A

120176786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475203-C-T

120176815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119475174-A-G

120177069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474946-A-G

120177090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474930-T-C

120177243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474818-G-A

120177243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474818-G-T

120177258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119474810-G-A

120177258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119474810-G-T

120177355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119474742-G-A

120177355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119474742-G-C

120177355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119474742-G-T

120177506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474614-G-A

120177638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474478-G-A

http://identifiers.org/hco/2/GRCh38#120177836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119474336-C-A

120177836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474336-C-T

120177907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474282-G-T

120177930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119474260-G-T

120178447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473398-T-G

120178645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473211-A-G

120178664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473197-A-T

120178701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473160-A-G

120178774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473115-A-G

120178774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473115-A-T

120178826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473070-T-A

120178834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119473040-G-C

http://identifiers.org/hco/2/GRCh38#120178918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#119472957-C-A

120179071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19819
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119472807-G-T