97307384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45890365-G-T

97307389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45890370-G-A

97307389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45890370-G-C

97307389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45890370-G-T

97307396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45890377-G-A

97307453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45890426-G-A

97307453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45890426-G-C

97307453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45890426-G-T

97307571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890505-T-A

97307589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890523-T-A

97307589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890523-T-C

97307589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890523-T-G

97307590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890524-G-T

97307658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890562-T-A

97307658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890562-T-C

97307709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45890608-A-G

97307777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45890686-C-T

http://identifiers.org/hco/9/GRCh38#97307800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45890711-A-C

97307843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45890733-A-G

97307843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45890733-A-T

http://identifiers.org/hco/9/GRCh38#97307867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45890740-C-A

97308139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45890956-G-A

97308139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45890956-G-C

http://identifiers.org/hco/9/GRCh38#97308173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45890985-C-A

97308173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890985-C-G

97308173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890985-C-T

97308185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45890997-T-C

97308527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892001-C-T

97308544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892043-A-G

97308565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892064-G-A

97308585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892092-A-G

97308613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892117-A-G

97308639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892140-G-A

97308678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892166-A-G

97308921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892385-C-T

http://identifiers.org/hco/9/GRCh38#97308937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45892401-A-C

97308995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892771-A-G

97309122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45892923-A-G

97309198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893007-T-G

97309276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893069-G-A

97309276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893069-G-T

97309333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893137-A-G

97309333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893137-A-T

97309416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 45893218-G-A

97309440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45893242-C-T

97309566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45893368-C-T

97309599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45893401-C-T

97309685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893464-T-A

97309685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893464-T-G

97309690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893469-A-G

http://identifiers.org/hco/9/GRCh38#97309704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45893483-A-C

97309704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893483-A-T

97309714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893493-T-A

97309714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893493-T-C

97309714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893493-T-G

http://identifiers.org/hco/9/GRCh38#97309729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45893508-A-C

97309737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893516-T-A

http://identifiers.org/hco/9/GRCh38#97309747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45893528-C-A

97309865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893625-C-T

http://identifiers.org/hco/9/GRCh38#97309966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45893708-A-C

97310057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45893800-G-C

97310088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45894061-C-G

97311344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45894751-A-G

97311523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45894905-C-T

97311688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45895050-A-G

http://identifiers.org/hco/9/GRCh38#97311808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45895905-C-A

97311832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45895926-T-C

97311855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45895949-G-C

97311965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896059-T-C

97311988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896083-G-A

97311988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896083-G-T

97312002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896091-G-T

http://identifiers.org/hco/9/GRCh38#97312091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45896141-C-A

97312091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896141-C-G

97312152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45896203-T-C

97312155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45896206-G-C

97312257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896311-G-A

97312270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896324-A-T

http://identifiers.org/hco/9/GRCh38#97312306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45896348-C-A

97312306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896348-C-T

97312495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896505-C-T

97312546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45896551-A-G

http://identifiers.org/hco/9/GRCh38#97313115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45898434-C-A

97313306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45898627-T-C

97313333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45898654-G-A

97313333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45898654-G-T

http://identifiers.org/hco/9/GRCh38#97313368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45898685-C-A

http://identifiers.org/hco/9/GRCh38#97313375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45898692-C-A

97313375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898692-C-T

97313408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898732-G-A

http://identifiers.org/hco/9/GRCh38#97313412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45898736-C-A

97313412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898736-C-G

97313412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898736-C-T

97313415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898739-A-G

97313415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898739-A-T

http://identifiers.org/hco/9/GRCh38#97313417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45898741-C-A

97313417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898741-C-G

97313450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898767-G-A

97313450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898767-G-T

97313451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898768-G-T

97313460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45898777-G-T

http://identifiers.org/hco/9/GRCh38#97313629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45898910-A-C

97314233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45899785-G-A

97314233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45899785-G-C

http://identifiers.org/hco/9/GRCh38#97314309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45899876-C-A

97314335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45899900-G-A

97314379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45899943-C-G

97314581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900126-C-T

97314626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45900170-G-A

97314722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45900266-C-G

97314722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45900266-C-T

97314816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900359-G-A

http://identifiers.org/hco/9/GRCh38#97314902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45900442-C-A

97314902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45900442-C-T

97315029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900539-G-A

97315033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900543-T-A

97315074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900584-G-A

97315074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900584-G-T

97315088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900598-T-C

97315096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900605-A-G

97315424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900862-T-A

97315565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45900967-T-C

97316176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45901599-G-T

http://identifiers.org/hco/9/GRCh38#97316234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45901664-A-C

97316343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45901766-G-A

97316458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45901882-G-A

97316508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45901951-A-G

97316691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902105-G-A

97316862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902266-C-T

97316928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902288-G-C

97316928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902288-G-T

97316986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902349-T-C

http://identifiers.org/hco/9/GRCh38#97316993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45902355-C-A

http://identifiers.org/hco/9/GRCh38#97317016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45902378-C-A

97317016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902378-C-T

http://identifiers.org/hco/9/GRCh38#97317017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45902379-C-A

97317017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902379-C-G

97317017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902379-C-T

97317029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902386-T-C

97317029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902386-T-G

97317053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902410-C-T

http://identifiers.org/hco/9/GRCh38#97317239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45902641-C-A

97317239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902641-C-G

97317239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902641-C-T

97317253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902663-T-C

97317414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45902992-A-G

97317478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45903039-A-G

http://identifiers.org/hco/9/GRCh38#97317517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45903082-C-A

97317620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45903173-A-G

97318078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45903566-T-C

http://identifiers.org/hco/9/GRCh38#97318277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45903702-A-C

97318369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45903790-G-T

97318626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904025-G-A

97318626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904025-G-T

97318661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904055-C-T

97318687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904078-G-A

97318687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904078-G-T

http://identifiers.org/hco/9/GRCh38#97318702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45904093-C-A

97318711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904102-T-A

97318711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904102-T-C

97318826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904213-G-A

97318826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904213-G-T

97320034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904455-T-A

http://identifiers.org/hco/9/GRCh38#97320104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45904516-C-A

97320104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904516-C-G

97320104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904516-C-T

97320232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904640-T-C

http://identifiers.org/hco/9/GRCh38#97320257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45904659-A-C

97320257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904659-A-G

97320304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904698-G-A

97320304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904698-G-C

97320569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45904943-G-T

http://identifiers.org/hco/9/GRCh38#97322738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45905882-C-A

97322738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45905882-C-T

97322905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45906081-A-G

97322905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45906081-A-T

97322944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906125-T-C

97323351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906427-T-C

97323359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906435-C-T

97323474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906550-T-G

http://identifiers.org/hco/9/GRCh38#97323625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45906706-C-A

97323625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906706-C-T

97323636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906715-T-G

97323727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906787-G-C

97323727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906787-G-T

97323735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906795-G-A

97323735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906795-G-C

97323735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906795-G-T

http://identifiers.org/hco/9/GRCh38#97323771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45906819-C-A

97323771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45906819-C-T

97323855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45906903-G-A

97323855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45906903-G-T

97324081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45907108-G-A

97324081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45907108-G-T

97324353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45907352-C-T

97324901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909141-G-T

97324918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909158-A-G

97324918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909158-A-T

97324952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909183-G-A

http://identifiers.org/hco/9/GRCh38#97324984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45909214-C-A

97325006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909246-T-C

97325120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45909360-G-A

97325120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45909360-G-C

97325127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45909367-G-A

97325127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45909367-G-C

97325292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909626-T-A

97325308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909642-G-A

97325325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909659-T-C

97325325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45909659-T-G

97325894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45910669-A-G

97326264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911015-C-T

97326280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911032-G-A

97326325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911077-G-A

97326370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911124-G-T

97326408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911161-T-C

http://identifiers.org/hco/9/GRCh38#97326467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45911198-C-A

97326534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911266-G-A

http://identifiers.org/hco/9/GRCh38#97326679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45911411-C-A

97326699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911431-A-G

97326703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911435-A-G

http://identifiers.org/hco/9/GRCh38#97326737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45911466-C-A

http://identifiers.org/hco/9/GRCh38#97326761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45911490-C-A

97326761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911490-C-T

97326777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911510-A-G

97326787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911520-T-A

97326787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911520-T-C

http://identifiers.org/hco/9/GRCh38#97326800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45911533-C-A

97326857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911590-T-C

97326857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911590-T-G

97326860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911593-A-G

97326860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911593-A-T

97327370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45911832-A-G

97327587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45912096-T-C

97327633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45912135-C-T

97327866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45912494-A-G

http://identifiers.org/hco/9/GRCh38#97327894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45912526-C-A

97327894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45912526-C-T

97328024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45912742-G-A

97328024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45912742-G-T

http://identifiers.org/hco/9/GRCh38#97328166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45912889-A-C

97328191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45912927-A-T

97328199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45912937-G-A

97328272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913017-G-T

97328276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913021-A-G

97328388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913768-T-G

97328457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913837-A-G

97329485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45913903-C-G

97330212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914263-A-G

97330229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914280-A-G

97330246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914297-T-G

97330291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914338-C-T

97330329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45914376-T-C

97330486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914521-A-G

http://identifiers.org/hco/9/GRCh38#97330541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45914576-A-C

97330541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914576-A-G

97330550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914585-A-G

97330558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914593-T-A

97330580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914615-T-C

97330582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914617-C-G

97330582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 45914617-C-T

97330609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914644-C-G

http://identifiers.org/hco/9/GRCh38#97330614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45914649-C-A

97330636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914671-G-A

97330636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914671-G-C

97330636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45914671-G-T

97330719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45914760-G-A

http://identifiers.org/hco/9/GRCh38#97330727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45914768-A-C

97330783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914896-A-G

97330783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914896-A-T

97330794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914907-G-A

97330875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45914986-G-T

97330895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915006-A-T

97342825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915672-C-T

97343044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915870-A-G

97343164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915966-T-G

97343189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45915991-T-C

http://identifiers.org/hco/9/GRCh38#97343274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45916107-C-A

97343340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45916195-G-A

97343366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45916218-G-A

97343471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45916327-C-G

97343471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45916327-C-T

97343481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45916336-A-G

97343493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45916342-G-A

97343648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916433-G-A

97343648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916433-G-C

97343648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916433-G-T

97343689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916442-A-G

97343689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916442-A-T

97343690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45916443-G-T

97347148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917226-G-A

97347148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917226-G-T

97347165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917243-A-G

http://identifiers.org/hco/9/GRCh38#97347171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45917248-C-A

http://identifiers.org/hco/9/GRCh38#97347191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45917268-A-C

97347191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917268-A-G

97347235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917308-A-G

97347235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917308-A-T

97347236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917309-C-G

97347236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45917309-C-T

97347479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45917554-C-T

97347571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45918174-G-C

97347571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45918174-G-T

97347580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45918183-G-T

97347758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45919240-G-A

97347758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45919240-G-T

97348027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45919411-A-G

97348282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45919617-G-T

97348364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45919658-T-C

http://identifiers.org/hco/9/GRCh38#97348483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45919750-A-C

97348759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920492-G-A

http://identifiers.org/hco/9/GRCh38#97348950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45920709-C-A

97348950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920709-C-T

97348975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920734-A-T

http://identifiers.org/hco/9/GRCh38#97348990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45920753-C-A

97348990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920753-C-T

http://identifiers.org/hco/9/GRCh38#97349030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45920792-C-A

97349030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45920792-C-T

97349108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45920841-C-T

97349218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45920951-G-A

97349218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45920951-G-T

97349238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45920971-C-T

http://identifiers.org/hco/9/GRCh38#97349277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45921010-C-A

97349277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45921010-C-T

97349484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921174-A-G

97349595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921284-G-A

97349603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921292-C-T

http://identifiers.org/hco/9/GRCh38#97349675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45921326-A-C

97349675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921326-A-G

97349867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45921488-A-G

97350404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45921892-C-T

http://identifiers.org/hco/9/GRCh38#97350479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45921967-C-A

97350479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45921967-C-T

97350499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45921987-G-A

97350611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922103-T-C

97353459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922297-T-C

97353596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922464-A-G

97353932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922737-G-C

97353952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922754-C-T

97353990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45922791-G-A

97354374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923009-T-A

97354374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923009-T-G

http://identifiers.org/hco/9/GRCh38#97354417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45923033-C-A

97354417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923033-C-T

97354508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923110-G-A

97354510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923112-G-T

97354572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45923167-G-A

97354698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45923293-T-G

97354742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923350-A-G

97354742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923350-A-T

97354855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923445-T-G

97354897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45923487-T-C

97354915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45923505-T-G

97355020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923610-T-G

97355022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923612-A-G

97355023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923613-T-C

97355024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923614-T-G

97355035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923625-G-T

http://identifiers.org/hco/9/GRCh38#97355097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45923686-C-A

http://identifiers.org/hco/9/GRCh38#97355099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45923688-C-A

97355099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923688-C-G

97355099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923688-C-T

97355583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923822-C-T

97355585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923824-C-T

97355628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923862-A-T

97355837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923991-C-T

97355838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923992-G-A

97355838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45923992-G-T

97355959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45924109-G-C

97355959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45924109-G-T

97355969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45924119-G-T

97356036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45924200-C-T

97356156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45924307-G-A

http://identifiers.org/hco/9/GRCh38#97357427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45925965-A-C

97357427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45925965-A-G

97357555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926098-T-C

97357697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45926240-C-G

97357750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45926292-G-A

97357752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45926294-G-A

http://identifiers.org/hco/9/GRCh38#97357769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45926311-C-A

http://identifiers.org/hco/9/GRCh38#97357777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45926319-A-C

97357837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45926358-G-A

97357837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45926358-G-T

97357841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45926362-T-G

http://identifiers.org/hco/9/GRCh38#97358246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45926582-A-C

97358246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926582-A-G

97358521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926689-G-A

97358521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926689-G-T

97358781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45926842-A-G

97359519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45927514-G-A

http://identifiers.org/hco/9/GRCh38#97359847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45927826-C-A

97359984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 45927946-A-G

97360062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45928024-C-T

97360186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928151-A-G

97360240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928197-G-A

97360240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928197-G-C

97360240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928197-G-T

97360486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45928420-G-A

97361340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929139-C-T

http://identifiers.org/hco/9/GRCh38#97361366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45929177-A-C

97361507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929324-G-A

97361507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929324-G-T

97361523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929343-G-A

http://identifiers.org/hco/9/GRCh38#97361623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45929453-C-A

97361623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929453-C-T

97361624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929454-A-G

97361645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929472-A-G

97361722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45929535-G-A

http://identifiers.org/hco/9/GRCh38#97361893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45929706-C-A

http://identifiers.org/hco/9/GRCh38#97362038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45929805-C-A

97362038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929805-C-T

http://identifiers.org/hco/9/GRCh38#97362064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45929820-C-A

97362064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45929820-C-T

97362227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45929982-T-C

http://identifiers.org/hco/9/GRCh38#97362553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45930309-A-C

97362553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45930309-A-G

97362767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45930637-A-G

97362980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45930805-G-A

97363406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45931169-G-A

97363760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45932192-G-A

97363760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45932192-G-T

http://identifiers.org/hco/9/GRCh38#97363773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45932207-C-A

97363773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45932207-C-T

http://identifiers.org/hco/9/GRCh38#97363817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45932250-C-A

97363817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45932250-C-T

97363872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45932293-G-A

97363872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45932293-G-T

http://identifiers.org/hco/9/GRCh38#97363933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45932343-C-A

97364081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45932485-G-A

97364375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45933425-G-T

97364397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45933461-A-G

97364397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45933461-A-T

97364433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45933501-T-C

97364520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45933593-T-C

97364520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45933593-T-G

http://identifiers.org/hco/9/GRCh38#97364583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45933655-C-A

97364583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45933655-C-T

http://identifiers.org/hco/9/GRCh38#97364598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45933668-C-A

http://identifiers.org/hco/9/GRCh38#97364671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45933736-C-A

97364671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45933736-C-T

http://identifiers.org/hco/9/GRCh38#97364672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45933737-A-C

97365002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940328-T-C

http://identifiers.org/hco/9/GRCh38#97365085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45940403-C-A

97365085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45940403-C-T

http://identifiers.org/hco/9/GRCh38#97365204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45940523-C-A

97365245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940553-A-G

97365320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940627-G-A

97365320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940627-G-T

97365371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940679-T-C

http://identifiers.org/hco/9/GRCh38#97365378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45940686-C-A

97365378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940686-C-T

97365381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940691-G-T

97365387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940697-A-G

97365424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940717-G-T

http://identifiers.org/hco/9/GRCh38#97365560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45940798-C-A

97365560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940798-C-T

97365640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940877-G-A

97365660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940897-G-A

97365660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45940897-G-C

97365786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941040-T-A

97366190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941510-C-T

97366314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941614-G-A

97366323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941622-C-G

97366323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941622-C-T

97366437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941700-C-T

97366441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941704-G-A

97366441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941704-G-T

http://identifiers.org/hco/9/GRCh38#97366451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45941709-C-A

97366451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941709-C-T

97366459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941721-G-A

97366459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941721-G-T

97366627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45941851-C-T

97366731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941960-A-G

http://identifiers.org/hco/9/GRCh38#97366763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45941999-C-A

97366763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941999-C-G

97366763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45941999-C-T

http://identifiers.org/hco/9/GRCh38#97366813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45942036-C-A

97366813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45942036-C-T

97366827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45942050-G-A

http://identifiers.org/hco/9/GRCh38#97366828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45942051-C-A

http://identifiers.org/hco/9/GRCh38#97366854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45942077-A-C

97369790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45944228-A-G

97370141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944536-A-G

97370151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944546-G-T

97370297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944638-A-G

97370326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944658-G-A

97370361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944692-C-T

97370452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944782-C-T

97370465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944792-C-G

http://identifiers.org/hco/9/GRCh38#97370582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45944881-A-C

97370582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944881-A-G

97370582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944881-A-T

97370583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45944882-G-C

97370682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45944982-C-T

97370740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45945040-C-T

http://identifiers.org/hco/9/GRCh38#97370781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45945081-C-A

97370798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945098-C-G

97370798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945098-C-T

http://identifiers.org/hco/9/GRCh38#97370806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45945106-C-A

97370846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945115-A-G

97370846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945115-A-T

97370856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945123-G-A

97370856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945123-G-T

97371004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945207-C-T

http://identifiers.org/hco/9/GRCh38#97371173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45945230-C-A

97371173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945230-C-G

97371173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945230-C-T

97371176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945233-G-A

97371176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945233-G-T

97371180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945237-G-A

97371180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945237-G-C

97371180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945237-G-T

97371217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945256-G-A

http://identifiers.org/hco/9/GRCh38#97371243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45945281-C-A

97371243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945281-C-G

97371243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945281-C-T

97371244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945282-G-A

97371264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945302-T-C

http://identifiers.org/hco/9/GRCh38#97371314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45945335-C-A

97371314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945335-C-G

97371314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945335-C-T

97371363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45945385-G-T

97371430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946048-G-T

http://identifiers.org/hco/9/GRCh38#97371439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45946057-C-A

97371439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946057-C-T

http://identifiers.org/hco/9/GRCh38#97371475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45946091-C-A

97371479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946095-G-T

97371494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946109-G-T

http://identifiers.org/hco/9/GRCh38#97371498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45946113-C-A

97371498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946113-C-G

97371498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946113-C-T

97371520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946132-A-G

97371520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946132-A-T

http://identifiers.org/hco/9/GRCh38#97371528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45946140-C-A

97371528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946140-C-T

97371544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946156-T-C

97371544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946156-T-G

http://identifiers.org/hco/9/GRCh38#97371732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45946338-C-A

97371732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946338-C-G

97371748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946354-T-C

http://identifiers.org/hco/9/GRCh38#97371767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45946381-C-A

97371767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946381-C-T

97371769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946383-G-A

97371769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946383-G-T

97371820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946430-G-C

97371820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45946430-G-T

http://identifiers.org/hco/9/GRCh38#97374453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45948665-C-A

97374479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45948692-G-A

97374479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45948692-G-T

http://identifiers.org/hco/9/GRCh38#97374490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45948703-C-A

97374490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45948703-C-T

97374506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45948712-G-C

97374601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45948808-C-T

97374643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45948850-A-G

97374702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948900-G-A

97374702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948900-G-C

97374702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948900-G-T

97374718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948917-T-G

97374722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948921-G-A

97374722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948921-G-T

http://identifiers.org/hco/9/GRCh38#97374748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45948947-C-A

97374748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948947-C-T

97374785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45948990-A-G

97375049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949159-G-A

97375191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949282-A-G

97375209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949301-C-T

97375212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949304-T-C

97375238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949332-C-T

97375242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949336-G-C

97375405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949417-T-C

97375422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45949434-C-T

97375517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45949513-A-G

97375559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45949555-G-A

97375559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 45949555-G-T

97375727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949619-G-A

97375727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949619-G-T

97375731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949623-G-T

http://identifiers.org/hco/9/GRCh38#97375852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45949755-C-A

97375852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949755-C-T

97375854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949757-T-C

97375854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949757-T-G

97375862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949768-G-A

97375862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949768-G-T

97375925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949820-T-C

97375951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949843-G-C

97375987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949865-T-C

97376014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949892-A-G

http://identifiers.org/hco/9/GRCh38#97376020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45949898-C-A

97376020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949898-C-G

97376020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949898-C-T

97376021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45949899-T-A

97376156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950024-C-G

97376156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950024-C-T

97376177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950043-G-T

http://identifiers.org/hco/9/GRCh38#97376193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950056-C-A

97376242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950105-G-C

97376242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950105-G-T

97376256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950119-G-T

97376300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950151-G-C

97376300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950151-G-T

http://identifiers.org/hco/9/GRCh38#97376316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950167-C-A

97376316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950167-C-G

97376316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950167-C-T

http://identifiers.org/hco/9/GRCh38#97376358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950209-C-A

97376358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950209-C-T

http://identifiers.org/hco/9/GRCh38#97376450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950295-A-C

97376450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950295-A-G

97376450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950295-A-T

http://identifiers.org/hco/9/GRCh38#97376491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950334-C-A

97376491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950334-C-T

97376545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950388-T-C

http://identifiers.org/hco/9/GRCh38#97376609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950449-C-A

97376629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950469-A-G

97376630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950470-A-G

97376658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45950497-T-C

http://identifiers.org/hco/9/GRCh38#97376876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950709-C-A

97376876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45950709-C-G

97376934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45950762-C-T

97377017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45950801-G-A

97377017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45950801-G-C

97377017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45950801-G-T

http://identifiers.org/hco/9/GRCh38#97377110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45950859-C-A

97377110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29303
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45950859-C-G