http://identifiers.org/hco/9/GRCh38#127505489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32815138-C-A

127505489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32815138-C-T

127505544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32815087-G-A

127505544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32815087-G-T

http://identifiers.org/hco/9/GRCh38#127505556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32815075-C-A

127505556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32815075-C-T

127505635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814998-A-G

127505635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814998-A-T

127505685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814961-T-A

127505685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814961-T-C

127505685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814961-T-G

127505730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814919-G-T

127505810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814857-T-C

127505814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814852-A-G

http://identifiers.org/hco/9/GRCh38#127505910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814771-C-A

127505910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814771-C-T

127505991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814725-G-A

127505991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814725-G-T

127506052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814699-G-A

http://identifiers.org/hco/9/GRCh38#127506133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814650-C-A

127506133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814650-C-G

127506133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814650-C-T

127506140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814642-A-G

http://identifiers.org/hco/9/GRCh38#127506141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814641-C-A

127506146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814636-T-C

http://identifiers.org/hco/9/GRCh38#127506206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814595-C-A

127506206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814595-C-G

127506206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814595-C-T

http://identifiers.org/hco/9/GRCh38#127506298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814546-C-A

127506298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814546-C-T

http://identifiers.org/hco/9/GRCh38#127506299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814545-C-A

127506299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814545-C-T

http://identifiers.org/hco/9/GRCh38#127506372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814471-A-C

127506372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814471-A-T

127506377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814463-T-C

127506390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814448-A-G

http://identifiers.org/hco/9/GRCh38#127506392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814446-C-A

127506392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814446-C-G

127506392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814446-C-T

127506430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814409-T-A

127506430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814409-T-C

http://identifiers.org/hco/9/GRCh38#127506439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814399-C-A

127506439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814399-C-T

127506449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32814389-G-A

127506449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32814389-G-T

http://identifiers.org/hco/9/GRCh38#127506463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814375-A-C

127506467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814361-A-G

http://identifiers.org/hco/9/GRCh38#127506492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814331-C-A

127506492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814331-C-T

http://identifiers.org/hco/9/GRCh38#127506493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814330-C-A

127506493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814330-C-T

http://identifiers.org/hco/9/GRCh38#127506519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814327-C-A

127506567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814291-A-G

127506677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814206-T-A

127506677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814206-T-C

http://identifiers.org/hco/9/GRCh38#127506712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32814171-C-A

127506712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814171-C-T

127506789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814095-C-T

127506801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32814082-A-T

127507035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32813849-G-T

127507212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32813672-A-G

127507284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32813588-C-T

127507287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32813585-C-G

127507287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32813585-C-T

127507298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32813574-G-A

127507304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 32813568-G-A

127507304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813568-G-C

http://identifiers.org/hco/9/GRCh38#127507320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32813552-C-A

127507326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32813546-A-G

http://identifiers.org/hco/9/GRCh38#127507352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32813520-C-A

127507352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 32813520-C-T

127507471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813414-T-G

http://identifiers.org/hco/9/GRCh38#127507494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32813404-A-C

127507494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813404-A-G

127507498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813403-T-A

127507498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813403-T-C

127507498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813403-T-G

127507529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813378-G-A

127507529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813378-G-T

127507534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813373-T-A

127507534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813373-T-C

127507534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813373-T-G

127507570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813349-G-A

127507570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32813349-G-T

127507911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32813124-T-A

127508039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32813018-G-C

127508062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812995-C-T

127508224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812842-G-A

127508224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812842-G-T

127508281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812806-A-G

http://identifiers.org/hco/9/GRCh38#127508284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32812803-C-A

127508284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812803-C-T

127508313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812775-G-A

127508313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812775-G-T

127508351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812752-G-A

127508351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812752-G-T

127508353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812750-T-C

127508549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812557-T-C

127508585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812535-C-T

127508651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812490-G-C

127508651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812490-G-T

127508654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812487-G-A

127508654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812487-G-T

127508828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812331-A-G

127508828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812331-A-T

127508926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812273-T-G

127509058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32812152-A-G

127509176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812052-G-A

127509176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812052-G-T

http://identifiers.org/hco/9/GRCh38#127509189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32812034-C-A

127509189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812034-C-T

127509206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812014-G-A

127509206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32812014-G-T

http://identifiers.org/hco/9/GRCh38#127509258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32811977-C-A

127509258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811977-C-G

http://identifiers.org/hco/9/GRCh38#127509259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32811976-C-A

127509264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811971-G-T

http://identifiers.org/hco/9/GRCh38#127509265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32811970-C-A

127509265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811970-C-T

127509456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811810-A-T

127509615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811666-G-A

127509637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811650-G-A

127509700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811463-T-C

127509748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811388-C-T

127509753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811383-G-A

http://identifiers.org/hco/9/GRCh38#127509758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32811378-C-A

127509758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811378-C-G

127509788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32811357-C-T

127509881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811337-T-A

127509954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811261-A-G

127509954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811261-A-T

http://identifiers.org/hco/9/GRCh38#127509959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32811256-C-A

127509959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811256-C-T

127509969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32811246-G-A

127509969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32811246-G-C

127509969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32811246-G-T

127510011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811225-C-G

127510011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32811225-C-T

127510061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32811207-G-A

127510061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32811207-G-T

127510086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32811182-T-A

http://identifiers.org/hco/9/GRCh38#127516913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32809819-C-A

127516913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32809819-C-T

127516931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32809801-G-A

127516937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32809795-T-C

127516961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32809771-A-G

127517024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32809708-G-A

127517042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809690-G-A

127517059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809673-C-T

http://identifiers.org/hco/9/GRCh38#127517066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32809666-C-A

127517066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809666-C-G

127517222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32809500-T-C

127517252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809470-G-C

127517334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809415-T-C

127517591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809308-C-T

127517648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809270-A-G

127517740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809195-C-T

http://identifiers.org/hco/9/GRCh38#127517760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32809186-C-A

127517760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809186-C-T

127517795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32809149-G-T

127518063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808908-T-C

127518349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32808727-C-T

127518485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32808596-C-G

127518690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32808436-T-C

http://identifiers.org/hco/9/GRCh38#127519293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32807924-A-C

127519349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32807872-G-T

127519564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32807696-C-T

127519976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32807341-G-C

127520067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32807251-C-T

127521677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32805026-C-T

127521893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804869-C-T

127521904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804863-T-C

http://identifiers.org/hco/9/GRCh38#127521982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32804778-C-A

127521982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804778-C-T

127521996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804764-G-A

127522638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804218-C-T

127522652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32804204-C-T

127523086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32803676-C-T

http://identifiers.org/hco/9/GRCh38#127523149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32803626-A-C

127523426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802830-G-A

http://identifiers.org/hco/9/GRCh38#127523484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32802773-C-A

http://identifiers.org/hco/9/GRCh38#127523570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32802685-C-A

127523570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802685-C-T

127523571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802684-T-C

127523571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802684-T-G

http://identifiers.org/hco/9/GRCh38#127523601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32802654-C-A

127523601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32802654-C-T

127523606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32802649-A-T

127523608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32802647-G-T

http://identifiers.org/hco/9/GRCh38#127523628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32802627-C-A

127523628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802627-C-T

127523668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802608-A-G

127523669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802607-G-A

127523669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802607-G-C

127523729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32802547-T-C

127523732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32802544-T-G

127523768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 32802508-G-A

127523782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32802494-G-A

127523782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32802494-G-C

127523782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 32802494-G-T

127523955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802394-G-T

127523995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802358-G-T

127524242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802148-C-T

127524378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32802019-G-A

127524454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32801947-C-G

127524454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32801947-C-T

127524656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32801803-C-T

http://identifiers.org/hco/9/GRCh38#127524950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32801560-C-A

127524950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32801560-C-G

http://identifiers.org/hco/9/GRCh38#127524977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32801536-A-C

http://identifiers.org/hco/9/GRCh38#127525004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32801509-C-A

127525004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32801509-C-T

127525078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32801436-A-G

http://identifiers.org/hco/9/GRCh38#127525209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32801305-A-C

127525209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801305-A-G

127525261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801246-G-A

127525261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801246-G-T

127525270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801237-G-A

127525270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32801237-G-T

127526794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800650-T-A

127526898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800569-G-C

127526966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800502-G-A

127527045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800410-G-A

127527045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800410-G-T

127527057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800395-T-C

127527061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800391-G-T

127527139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800039-G-A

127527139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800039-G-T

127527140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800038-G-A

127527140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800038-G-C

127527140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32800038-G-T

127527183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799998-C-T

127527240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32799941-C-T

http://identifiers.org/hco/9/GRCh38#127527425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32799694-C-A

127527425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799694-C-T

http://identifiers.org/hco/9/GRCh38#127527463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32799656-C-A

http://identifiers.org/hco/9/GRCh38#127527464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32799655-C-A

127527472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799647-C-G

127527536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799583-C-T

127527843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799329-G-A

127527843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799329-G-C

127527903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799277-G-A

127527903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799277-G-C

127527983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799226-C-T

127528097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799137-C-G

http://identifiers.org/hco/9/GRCh38#127528216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32799000-A-C

127528216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32799000-A-T

127528700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32798584-C-T

127528702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32798582-C-G

http://identifiers.org/hco/9/GRCh38#127528703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32798581-A-C

127529736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32797717-A-G

127529788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32797672-T-C

127529836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32797630-C-T

127529987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32797515-G-A

127531548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32795998-T-C

http://identifiers.org/hco/9/GRCh38#127531652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32795905-C-A

127531652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32795905-C-T

127531688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32795869-T-G

127531757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32795800-G-A

127531757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32795800-G-T

127534123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32794480-C-T

127534151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32794455-G-A

127534170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32794437-G-C

127534236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32794367-C-G

127534280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32794348-C-G

127536599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32792694-T-A

127536807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32792526-G-A

127536903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32792451-G-A

127537460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32792001-G-A

127537462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32791999-A-T

127537481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32791980-A-G

http://identifiers.org/hco/9/GRCh38#127537519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32791948-C-A

127537717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32791699-C-T

http://identifiers.org/hco/9/GRCh38#127537844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32791580-C-A

http://identifiers.org/hco/9/GRCh38#127537974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32791487-C-A

127538070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32791394-G-A

127538093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32791335-T-C

http://identifiers.org/hco/9/GRCh38#127538207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32791250-A-C

127539243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32790788-A-G

127539308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32790740-G-A

127539344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32790709-T-C

http://identifiers.org/hco/9/GRCh38#127539704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32790385-C-A

127540258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32789945-G-A

127540338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32789866-G-C

127540544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32789516-C-T

127540836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32789231-C-T

http://identifiers.org/hco/9/GRCh38#127540871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32789196-C-A

127540871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32789196-C-T

127540950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32789132-T-C

127541221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32788876-A-G

127541668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32788256-A-G

http://identifiers.org/hco/9/GRCh38#127541676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32788248-C-A

127541676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32788248-C-T

127541991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32788020-T-A

127542040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32787989-G-A

http://identifiers.org/hco/9/GRCh38#127542587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32787675-C-A

127542593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32787669-C-G

127543224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787201-G-A

127543225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32787200-A-G

127543624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786860-G-C

http://identifiers.org/hco/9/GRCh38#127543643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32786841-C-A

127543898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786609-C-G

127543912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786589-G-C

127544049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786450-G-A

127545420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786151-G-C

127545420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786151-G-T

127545535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32786059-G-C

127546009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785634-G-A

127546062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785586-G-A

127546062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785586-G-T

127546083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785564-C-T

127546084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785563-G-A

127546094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32785553-C-G

127548396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32784219-G-A

127549058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782987-G-A

127549224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782830-C-T

127549390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782724-C-T

127549405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782707-A-G

127549417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782695-A-G

127549718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32782485-A-G

127550563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781904-A-G

127551013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781490-C-T

127554419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781109-G-A

127554422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32781106-T-C

http://identifiers.org/hco/9/GRCh38#127554531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32780993-C-A

127554531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32780993-C-T

http://identifiers.org/hco/9/GRCh38#127554542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32780982-C-A

127554542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32780982-C-T

127555426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32780389-G-A

127556441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32779652-T-A

127557730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778632-C-T

127557800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778567-C-T

127557840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778527-T-C

127557906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778466-G-A

127558113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778263-T-C

http://identifiers.org/hco/9/GRCh38#127558384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32778048-A-C

127558384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778048-A-G

127558426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32778024-T-C

127559187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32776373-A-G

127559311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32776252-T-C

127559442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32776146-C-T

127560234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32775159-T-C

127560306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32775087-A-G

127560400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32775028-T-C

http://identifiers.org/hco/9/GRCh38#127560493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32774936-C-A

127560493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32774936-C-T

127560875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32774263-C-T

127560876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32774262-C-T

127561021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32774126-T-C

http://identifiers.org/hco/9/GRCh38#127561041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32774106-C-A

127561047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32774101-T-A

127561160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32774042-A-G

http://identifiers.org/hco/9/GRCh38#127561192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32774011-C-A

127561192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32774011-C-T

http://identifiers.org/hco/9/GRCh38#127561210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32773990-C-A

127561336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32773916-A-G

http://identifiers.org/hco/9/GRCh38#127561362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32773890-C-A

127561386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32773866-A-G

127561848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32772838-G-A

127561956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32772783-G-A

127562093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32772645-G-A

127562224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32772518-C-T

127562328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32772418-C-T

127562330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32772416-A-G

127562350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32772396-T-A

127562670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32771742-G-C

127562744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32771666-C-T

127562970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32771468-A-T

127563009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32771425-G-A

127563168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32771270-C-T

127563303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32771147-G-C

127563398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32771073-G-A

127566475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32768755-A-G

127566536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32768694-C-T

127566832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32768444-T-C

127567748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32767597-T-C

127567830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32767494-A-G

127567932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32767345-G-A

127567965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32767266-G-C

127568608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32766611-C-T

http://identifiers.org/hco/9/GRCh38#127568705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32766514-C-A

127568705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32766514-C-T

http://identifiers.org/hco/9/GRCh38#127568721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32766498-C-A

127568721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32766498-C-T

http://identifiers.org/hco/9/GRCh38#127568734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32766485-C-A

127568734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32766485-C-T

127568885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32766349-T-A

127568885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32766349-T-C

127568935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32766317-G-A

127568935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32766317-G-T

127568990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32766278-G-A

127569031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32766235-G-A

127569031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32766235-G-C

127569031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32766235-G-T

http://identifiers.org/hco/9/GRCh38#127569128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32766175-A-C

127569128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: 32766175-A-G

127569171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32766162-C-G

http://identifiers.org/hco/9/GRCh38#127569646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32765800-A-C

127569802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: 32765580-A-G

127570145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: 32765300-T-G

127570418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32764522-C-G

127570418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32764522-C-T

127570594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32764374-C-G

127570594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32764374-C-T

127571029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32763984-C-T

127571061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32763942-G-C

127571112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32763890-G-C

http://identifiers.org/hco/9/GRCh38#127571360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32763723-A-C

127571429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32763667-G-A

127573139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32762574-G-A

127573139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32762574-G-C

http://identifiers.org/hco/9/GRCh38#127573360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32762399-C-A

127573360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: 32762399-C-T

127573424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32762351-T-C

http://identifiers.org/hco/9/GRCh38#127574634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32760182-C-A

http://identifiers.org/hco/9/GRCh38#127574738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32760076-A-C

127574844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32759982-T-C

http://identifiers.org/hco/9/GRCh38#127575026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32759802-A-C

127575916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32759271-G-A

127578910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: intron variant
orthologous variants: 32757822-C-T

127578950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32757788-G-A

127578950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25282
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32757788-G-C