http://identifiers.org/hco/12/GRCh38#119174294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116566420-C-A

119174333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116566384-T-C

http://identifiers.org/hco/12/GRCh38#119174411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116566325-C-A

http://identifiers.org/hco/12/GRCh38#119174417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116566319-C-A

119174524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116566224-A-G

119174525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116566223-G-C

119174525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116566223-G-T

119174609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116566149-A-G

119174775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116565940-G-A

119174845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116565882-C-G

119175300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564856-G-A

http://identifiers.org/hco/12/GRCh38#119175357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116564820-C-A

119175479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564613-G-A

119175489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564603-T-C

119175548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564549-C-T

119175686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564445-C-T

119175690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564441-G-A

119175691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564440-T-A

119175791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116564230-G-A

119176339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116563691-A-G

http://identifiers.org/hco/12/GRCh38#119176362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116563668-C-A

119176378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563628-A-G

119176378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563628-A-T

119176388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116563618-A-G

119176403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563603-T-C

119176410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116563596-A-G

http://identifiers.org/hco/12/GRCh38#119176415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116563591-C-A

http://identifiers.org/hco/12/GRCh38#119176500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116563511-C-A

119176500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563511-C-T

119176503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563508-G-A

119176503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563508-G-C

119176503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563508-G-T

http://identifiers.org/hco/12/GRCh38#119176628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116563392-C-A

119176628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563392-C-T

119176688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563340-G-A

http://identifiers.org/hco/12/GRCh38#119176980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116563097-C-A

119177075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116563016-G-A

119177147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116562955-C-T

119177152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116562950-A-G

119177273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116562827-A-G

119178331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561475-C-T

119178352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561462-T-C

119178392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561421-A-G

119178394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561419-A-G

http://identifiers.org/hco/12/GRCh38#119178522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116561340-C-A

119178522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561340-C-T

119178669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561200-T-C

119178714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561147-T-C

119178715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561146-G-C

119178715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561146-G-T

119178770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561092-G-A

119178770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116561092-G-T

119178950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116560904-G-A

119178950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116560904-G-T

119178979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116560873-T-C

119179066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560796-C-T

119179069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560793-T-G

119179078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560781-G-T

119179080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560779-A-G

119179144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560708-G-A

119179144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560708-G-T

http://identifiers.org/hco/12/GRCh38#119179205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116560657-C-A

119179205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560657-C-T

119179298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560551-A-G

http://identifiers.org/hco/12/GRCh38#119179300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116560549-C-A

119179300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116560549-C-T

119179436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 116560413-G-T

119179762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116560049-G-A

119179762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116560049-G-C

119180177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116559723-T-C

119180189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116559711-C-T

119180191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116559709-G-C

119180309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116559575-G-T

119181642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116558608-A-G

119181946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116558324-C-G

119181946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116558324-C-T

119182059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116558243-C-T

119182110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116558192-T-C

http://identifiers.org/hco/12/GRCh38#119182117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116558185-C-A

119182167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116558133-T-C

119182772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557850-G-A

119182810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557812-G-A

119182810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557812-G-T

119182868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557744-A-G

http://identifiers.org/hco/12/GRCh38#119182898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116557706-C-A

119182915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557689-T-C

119182964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557651-T-C

119182993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557616-G-A

119182993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557616-G-T

119183030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557580-G-A

119183030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557580-G-T

119183063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557549-T-C

119183065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557547-A-G

119183066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557546-A-G

http://identifiers.org/hco/12/GRCh38#119183074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116557534-C-A

119183074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116557534-C-T

119183320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557309-T-A

119183320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557309-T-C

119183347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557282-T-C

http://identifiers.org/hco/12/GRCh38#119183396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116557221-C-A

http://identifiers.org/hco/12/GRCh38#119183413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116557182-C-A

119183452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116557124-A-G

119183824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116556603-C-T

119184507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116555689-G-A

119184603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116555614-T-C

119186027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116554437-T-C

119186363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116554102-C-T

119186447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116554030-A-G

119186472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116554004-G-A

119186532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553953-C-T

119186593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553900-C-T

119186649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553845-C-T

http://identifiers.org/hco/12/GRCh38#119186659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116553835-C-A

119186659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553835-C-G

119186659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553835-C-T

119186670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553819-G-A

119186691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553798-G-A

119186691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553798-G-T

119186768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553760-T-A

119186772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553756-T-G

119186845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553686-G-A

119186845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553686-G-T

119186902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553641-T-G

http://identifiers.org/hco/12/GRCh38#119186932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116553614-C-A

119186932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553614-C-T

119186952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553601-G-T

119186976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553577-A-G

119186976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553577-A-T

119187000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 116553553-C-G

119188203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552252-C-G

119188619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552161-A-T

119188643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552133-T-C

119188779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116552043-G-A

119190643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548758-A-G

http://identifiers.org/hco/12/GRCh38#119190914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116548475-C-A

119190914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116548475-C-T

119191429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116547970-C-T

119193649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 116547600-T-C

119193820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116547426-G-A

http://identifiers.org/hco/12/GRCh38#119193879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116547367-C-A

119193879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547367-C-T

119193979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547266-G-A

119193979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547266-G-T

119194034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547214-G-A

119194034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547214-G-C

119194034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547214-G-T

119194211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116547039-G-A

http://identifiers.org/hco/12/GRCh38#119194380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116546892-C-A

119194380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546892-C-T

119194459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546834-A-G

119194459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546834-A-T

119194498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546796-T-A

119194498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546796-T-C

119194498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546796-T-G

http://identifiers.org/hco/12/GRCh38#119194528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116546767-C-A

119194528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546767-C-T

119194566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546732-T-C

119194566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546732-T-G

http://identifiers.org/hco/12/GRCh38#119194578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116546720-C-A

119194579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116546719-A-G

http://identifiers.org/hco/12/GRCh38#119194598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116546700-C-A

119194683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116546605-A-T

119194715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 116546582-T-G

http://identifiers.org/hco/12/GRCh38#119194748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116546549-C-A

119194748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116546549-C-T

119198980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116544730-G-T

119199037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116544673-C-T

119199152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116544560-G-A

119199345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116544385-G-A

119201849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541954-G-A

119201849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541954-G-C

119201849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541954-G-T

119201900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541906-C-T

119202106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541716-G-A

119202243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541545-G-A

119202393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541430-A-G

119202410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541419-G-A

119202519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541305-G-A

119202568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116541266-A-G

119204133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116536006-G-A

http://identifiers.org/hco/12/GRCh38#119204152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116535984-C-A

119204155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116535981-G-T

119204318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116535785-C-T

119204369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116535740-A-T

119204580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116535244-G-A

119204732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534955-T-A

119204890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534806-G-A

119204941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534757-G-C

119205038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534659-T-G

119205248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534506-G-C

119205481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534286-T-C

119206440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116534027-G-T

119206575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116533900-C-T

119206624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116533846-C-T

119206845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116533503-C-T

119207051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116533274-G-A

119207354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116532974-T-C

119207708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116532153-G-T

119207747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116532116-C-T

http://identifiers.org/hco/12/GRCh38#119208023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116531805-A-C

119208034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116531794-C-G

119208282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116531342-C-T

119208287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116531337-C-T

119208444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116531234-G-T

119208682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116531009-C-T

119208969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116530709-G-A

http://identifiers.org/hco/12/GRCh38#119208982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116530696-C-A

119208993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116530685-T-C

119209086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116530618-G-A

119209272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116530456-A-G

119211598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528674-G-T

119212035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528295-C-T

http://identifiers.org/hco/12/GRCh38#119212073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116528260-A-C

119212109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528224-T-G

119212152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528181-G-C

119212154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528179-T-C

119212231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528100-T-A

119212237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528094-G-A

119212237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116528094-G-T

119212373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116527968-A-G

119212374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116527967-G-A

119213127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116527231-G-A

119213306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116526323-G-A

119213306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116526323-G-T

119213334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116526295-T-C

119213380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116526254-A-T

http://identifiers.org/hco/12/GRCh38#119213509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116526146-C-A

http://identifiers.org/hco/12/GRCh38#119213568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116526104-C-A

119213680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116526021-A-G

119213686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116526015-T-C

119213726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116525992-A-G

119213865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116525862-T-C

119214982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524956-G-A

119215107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524823-G-A

http://identifiers.org/hco/12/GRCh38#119215284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116524662-C-A

119215285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524661-A-T

119215434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524523-T-A

119215451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524506-G-A

119215483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524474-T-C

http://identifiers.org/hco/12/GRCh38#119215488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116524462-A-C

119215502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524448-C-G

119215725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524244-C-G

119216228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116524076-A-G

119216350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523944-C-T

119216435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523886-A-G

http://identifiers.org/hco/12/GRCh38#119216494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116523822-A-C

119216494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523822-A-G

119216584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523729-G-C

119216830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523514-A-G

119216832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523512-T-C

119216957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523411-T-G

119216971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523398-T-C

http://identifiers.org/hco/12/GRCh38#119217039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116523336-A-C

119217065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523310-G-A

119217074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523301-T-C

119217103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116523270-A-G

http://identifiers.org/hco/12/GRCh38#119219930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

http://identifiers.org/hco/12/GRCh38#119220116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

119220221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

119220229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

119220229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

119220333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

119220393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116518494-G-A

119220487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 116518394-G-A

119220783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116518116-A-G

119220920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 116517986-A-G

119220922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 116517984-T-C

119220966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116517938-A-G

119221026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116517908-T-G

119221041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 116517890-G-T

119221191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116517744-C-T

119221236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116517682-A-G

http://identifiers.org/hco/12/GRCh38#119221371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#116517565-C-A

119221371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116517565-C-G

119221422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30171
most severe consequence: intron variant
orthologous variants: 116517512-C-G