http://identifiers.org/hco/12/GRCh38#12474151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134692369-C-A

12474465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692645-C-T

12474483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692662-T-A

http://identifiers.org/hco/12/GRCh38#12474585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134692742-C-A

12474608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692762-T-C

12474641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692795-A-T

12474643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692797-G-A

12474643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692797-G-T

12474760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692921-A-G

http://identifiers.org/hco/12/GRCh38#12474764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134692925-C-A

12474830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134692997-G-A

12474962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693119-C-T

http://identifiers.org/hco/12/GRCh38#12475269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134693413-C-A

12475269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693413-C-G

12475272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693416-A-G

http://identifiers.org/hco/12/GRCh38#12475327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134693468-A-C

http://identifiers.org/hco/12/GRCh38#12475433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134693578-C-A

12475433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693578-C-T

12475447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693592-T-A

12475447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693592-T-C

12475536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693669-G-T

12475631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693754-C-T

12475848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693884-G-T

http://identifiers.org/hco/12/GRCh38#12475954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134693988-A-C

http://identifiers.org/hco/12/GRCh38#12475961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134693994-A-C

12475961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134693994-A-G

12476013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694062-G-C

12476013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694062-G-T

12476470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694484-A-G

12476516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694523-T-C

http://identifiers.org/hco/12/GRCh38#12476621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134694650-C-A

12476621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694650-C-T

http://identifiers.org/hco/12/GRCh38#12476649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134694674-C-A

12476649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694674-C-G

12476649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3 prime UTR variant
orthologous variants: 134694674-C-T

12477390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 134695404-T-C

http://identifiers.org/hco/12/GRCh38#12477395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134695409-C-A

12477422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 134695436-T-A

12477478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 134695492-T-C

12477542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 134695556-T-C

12477865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 134695864-A-G

12478076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696074-T-C

http://identifiers.org/hco/12/GRCh38#12478087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134696083-A-C

12478087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696083-A-G

12478088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696084-A-G

12478095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696091-A-G

12478098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696094-G-T

12478133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696127-G-A

12478133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696127-G-T

http://identifiers.org/hco/12/GRCh38#12478292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134696245-A-C

12479401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696675-G-A

http://identifiers.org/hco/12/GRCh38#12479422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134696700-A-C

http://identifiers.org/hco/12/GRCh38#12479659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134696925-C-A

12479663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696929-C-T

12479670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134696936-T-C

12479740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697081-C-G

12480012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697259-G-A

12480210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697444-T-C

12480285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 134697519-G-A

12480285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 134697519-G-C

http://identifiers.org/hco/12/GRCh38#12480395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134697624-C-A

12480395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697624-C-T

12480444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697683-C-G

12480444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697683-C-T

http://identifiers.org/hco/12/GRCh38#12480445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134697684-C-A

12480445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697684-C-T

12480462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697701-C-T

12480464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697703-G-A

12480529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697766-C-T

12480564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134697802-G-A

12481024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134698142-A-G

12481090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134698159-C-T

12481621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134698744-T-C

12481695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134698796-C-G

http://identifiers.org/hco/12/GRCh38#12481734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134698824-A-C

http://identifiers.org/hco/12/GRCh38#12486279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134702123-C-A

12486525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134702286-C-G

http://identifiers.org/hco/12/GRCh38#12486566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134702325-C-A

12486566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134702325-C-T

12486587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134702352-T-A

12486659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134702420-C-T

12486805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134702565-T-G

12486903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134702661-T-C

12486987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134702722-C-T

12487243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134703007-T-C

12487251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134703015-G-A

12487251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134703015-G-C

12487251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134703015-G-T

12487319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134703284-G-A

12487319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134703284-G-T

12490923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134707352-A-T

12491208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134707608-G-A

12491429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134707859-G-A

12491451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 134707881-G-A

http://identifiers.org/hco/12/GRCh38#12491554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134707970-C-A

12491694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708104-G-A

12491694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708104-G-T

12491710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708120-T-C

12491712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708122-G-C

http://identifiers.org/hco/12/GRCh38#12491743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134708150-C-A

12491743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708150-C-G

12491916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708287-C-G

12492119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708488-A-G

12492128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708498-G-C

12492360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708770-A-G

12492407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708818-C-G

12492444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708855-G-A

12492444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708855-G-C

12492483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708895-C-G

12492483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134708895-C-T

12492595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134709003-A-G

12493577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134709966-A-G

12493587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134709976-G-A

12493899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134710306-C-T

12493983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134710346-T-C

12494374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134710754-G-A

12495956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712608-A-G

http://identifiers.org/hco/12/GRCh38#12496018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134712649-A-C

12496044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712677-G-A

12496050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712682-T-G

12496113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712727-T-C

12496160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712775-A-G

12496161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712776-T-A

12496161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712776-T-C

12496338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134712949-T-C

12496550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134713106-C-T

http://identifiers.org/hco/12/GRCh38#12496604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134713161-C-A

12497091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134713692-T-C

12497144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134713742-G-A

12498005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134715370-A-G

12499782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716076-G-A

12499924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716221-T-C

12500072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716359-C-T

12500098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716384-G-C

12500112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716394-A-G

12500143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716426-T-C

12500163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716446-T-C

12500217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716479-T-C

12500389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716647-G-T

12500396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716656-A-G

12500396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716656-A-T

12500510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134716766-A-G

12500549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 134716805-A-G

12500794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134717069-T-C

12500804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134717077-T-C

12500865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134717138-A-G

12503150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134718774-T-C

12503193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134718817-T-A

http://identifiers.org/hco/12/GRCh38#12504110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134719356-A-C

http://identifiers.org/hco/12/GRCh38#12506039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134720642-C-A

http://identifiers.org/hco/12/GRCh38#12506052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134720655-A-C

http://identifiers.org/hco/12/GRCh38#12506055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134720658-C-A

http://identifiers.org/hco/12/GRCh38#12506081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134720684-C-A

12506082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134720685-A-G

12506125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134720728-G-A

12506125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 134720728-G-T

http://identifiers.org/hco/12/GRCh38#12506166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134720768-C-A

12506234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, undefined
orthologous variants: 134720834-T-G

12506412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134721018-T-C

12506615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134721173-C-T

12506619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134721177-C-G

12506627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134721185-T-A

12506645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134721203-T-C

12506797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134721310-T-C

12509602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134725071-T-C

12509877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134725331-C-T

12510020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134725470-T-A

12510282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, undefined
orthologous variants: 134725699-G-A

12510297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, undefined
orthologous variants: 134725714-C-T

12510775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134727413-G-A

12511176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134727846-A-G

12511310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134727964-G-A

12511310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134727964-G-C

http://identifiers.org/hco/12/GRCh38#12511744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134728727-C-A

12512104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134729013-C-T

12512143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134729051-C-G

12512589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134729521-G-A

12513097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134730133-C-T

12513204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134730177-A-G

12513375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134730351-C-G

12513390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134730366-A-G

12513508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134730883-C-T

12513571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134730936-G-C

12513827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134731526-C-T

12513859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134731569-A-G

12513972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134731693-G-T

12514603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134732229-C-G

12514603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134732229-C-T

12514617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134732250-G-A

12518264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134733734-C-T

12518813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134734356-T-A

12518813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134734356-T-C

12518915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134734470-C-G

12519340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134734990-C-T

12519608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134735294-G-A

12519655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134735356-G-A

12519812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134735533-A-G

12520140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134736221-G-A

12520140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134736221-G-T

http://identifiers.org/hco/12/GRCh38#12521314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134738251-C-A

12521668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134738585-C-T

12521817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134738730-T-A

12521935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134738826-G-A

12522081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134738894-T-G

12522192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134738975-G-A

12522425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134739180-G-A

12522563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134739320-G-A

12523544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134740252-T-C

12523659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134740366-G-C

http://identifiers.org/hco/12/GRCh38#12524257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134740906-A-C

12524277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134740925-G-A

12524277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134740925-G-T

12524397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134741035-G-C

12526185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134743124-A-G

12526206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134743145-T-G

12526550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134743438-T-C

12526577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134743470-T-C

12526662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134743814-T-C

12526789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134743936-G-C

12526916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744018-C-T

12527119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744147-T-C

12527175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744197-C-G

12527240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744252-T-C

12527313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744339-C-T

http://identifiers.org/hco/12/GRCh38#12527697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134744610-C-A

12527849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744757-A-G

12528066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744940-A-T

12528077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134744951-T-C

12528157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134745039-C-T

http://identifiers.org/hco/12/GRCh38#12528246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134745115-A-C

12528246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134745115-A-G

12528321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134745189-G-T

12528617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134745415-T-C

http://identifiers.org/hco/12/GRCh38#12530609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134748777-A-C

12530921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134749295-G-C

12530975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134749332-G-A

12533357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134750987-T-C

http://identifiers.org/hco/12/GRCh38#12533439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#134751070-C-A

12533439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134751070-C-T

12533550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134751182-C-T

12533706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751375-T-C

12533741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751414-G-T

12534091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751753-G-A

12534091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751753-G-T

12534183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751793-C-T

12534186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751796-C-T

12534305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751935-G-A

12534323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134751953-C-T

12534564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134752148-G-T

12534614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134752201-G-C

12534755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134752364-C-T

12535305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134753594-T-C

12535479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134753752-G-C

12536069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134754454-G-A

12536069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134754454-G-C

12536129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134754500-T-C

12536135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134754506-A-T

12536418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134754786-T-C

12536488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134754860-T-C

http://identifiers.org/hco/12/GRCh38#12536499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134754871-C-A

http://identifiers.org/hco/12/GRCh38#12536557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134754909-C-A

http://identifiers.org/hco/12/GRCh38#12536746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134755194-C-A

12537607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134755910-C-T

12537892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134756190-A-G

http://identifiers.org/hco/12/GRCh38#12537901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134756200-A-C

12549659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134761376-C-T

http://identifiers.org/hco/12/GRCh38#12549682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134761399-A-C

12549726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134761436-T-G

http://identifiers.org/hco/12/GRCh38#12549763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134761468-A-C

http://identifiers.org/hco/12/GRCh38#12554511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134763074-A-C

12554602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134763148-G-C

12554602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 134763148-G-T

12554884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763340-C-T

12554948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763408-G-A

12554993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763446-T-C

12555026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763472-C-G

12555103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763546-G-A

12555119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763559-A-G

12555176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763619-G-A

12555261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763744-T-C

http://identifiers.org/hco/12/GRCh38#12555280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134763763-A-C

http://identifiers.org/hco/12/GRCh38#12555442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134763891-C-A

12555442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134763891-C-G

12559052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134766308-G-T

12559089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134766345-T-C

12559131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134766388-T-G

12559211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134766457-T-C

http://identifiers.org/hco/12/GRCh38#12559343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134766595-C-A

12559690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134766933-A-G

12559822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134767071-T-C

12559868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134767154-T-C

12559933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134767244-A-G

12560488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134767766-T-A

12560488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134767766-T-C

12560599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 134767878-C-T

12560734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 134767999-T-C

12560813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 134768075-T-C

http://identifiers.org/hco/12/GRCh38#12560961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#134768175-C-A

12560969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, undefined
orthologous variants: 134768182-G-A

12560969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, undefined
orthologous variants: 134768182-G-C

12560969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron_variant, undefined
orthologous variants: 134768182-G-T

12561155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134768352-T-C

12561569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134768803-G-T

12561596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134768844-G-C

12561597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134768845-G-A

12561941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: intron variant
orthologous variants: 134769155-C-T

12562157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5 prime UTR variant
orthologous variants: 134769277-G-A

12562314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5 prime UTR variant
orthologous variants: 134769345-G-T

12562695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5 prime UTR variant
orthologous variants: 134769693-G-A

12562762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5 prime UTR variant
orthologous variants: 134769760-G-A

12562787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17909
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 134769768-G-T