110149016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3 prime UTR variant
orthologous variants: 11248480-T-C

110149196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11248672-C-T

110149221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11248697-C-T

110149577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11249011-A-G

http://identifiers.org/hco/13/GRCh38#110149799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11249247-A-C

110150015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11249422-A-T

110150137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 11249546-G-T

http://identifiers.org/hco/13/GRCh38#110150154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11249565-A-C

110150405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11249843-G-A

http://identifiers.org/hco/13/GRCh38#110150432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11249870-C-A

110150432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11249870-C-T

110150517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11249984-G-T

110150712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11250270-C-T

110150915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11250495-A-G

110150926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11250506-G-A

110151177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11250727-A-G

110151342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11250871-T-C

110151373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11250907-C-T

110151612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11251091-A-T

110152016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11251395-G-A

110152131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11251505-C-T

110152459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11251783-G-A

110152459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11251783-G-T

http://identifiers.org/hco/13/GRCh38#110152638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11251955-C-A

110152638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11251955-C-G

110152638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11251955-C-T

http://identifiers.org/hco/13/GRCh38#110155217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11252832-C-A

110155246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11252859-T-A

110155253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11252866-G-A

110155253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11252866-G-T

110155266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11252878-T-C

http://identifiers.org/hco/13/GRCh38#110155289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11252900-A-C

110155322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11252933-G-A

110155322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11252933-G-C

110155422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253034-G-A

110155422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253034-G-C

110155422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253034-G-T

110155453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253044-T-C

110155469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253060-T-G

110155510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253094-T-C

110155528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253108-A-G

http://identifiers.org/hco/13/GRCh38#110155537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11253117-C-A

110155588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253166-G-A

110156548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253293-A-G

http://identifiers.org/hco/13/GRCh38#110156746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11253495-C-A

110156810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253543-G-A

110156866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253632-G-A

110156870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253636-G-C

110156874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253640-C-G

110156874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11253640-C-T

110157809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11254379-T-G

110161172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11256206-C-T

110161257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11256291-G-C

110161304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11256338-C-G

110161304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11256338-C-T

110161391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256425-G-A

110161391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256425-G-T

110161480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256522-C-T

110161508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256550-T-A

110161778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256749-G-A

http://identifiers.org/hco/13/GRCh38#110161815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11256795-A-C

110161815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256795-A-G

http://identifiers.org/hco/13/GRCh38#110161891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11256870-C-A

http://identifiers.org/hco/13/GRCh38#110161894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11256884-C-A

http://identifiers.org/hco/13/GRCh38#110161912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11256904-A-C

110161912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256904-A-G

110161913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11256905-G-A

110161977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11256970-T-G

110161984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11256977-T-C

110161984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11256977-T-G

110162073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11257065-G-A

110162073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11257065-G-T

110162189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11257165-C-T

110162456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257420-G-T

110162457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257421-A-T

110162464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257428-A-G

110162575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257545-A-T

http://identifiers.org/hco/13/GRCh38#110162584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11257555-A-C

110162584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257555-A-G

110162585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257556-A-T

110163108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11257937-T-C

110163205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258039-C-T

110163263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258090-A-G

110163296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258106-C-G

110163336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258144-G-T

http://identifiers.org/hco/13/GRCh38#110163416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11258222-C-A

http://identifiers.org/hco/13/GRCh38#110163590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11258360-C-A

110163590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258360-C-T

110163661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258416-A-G

110163796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258594-C-T

110164289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258955-C-T

110164300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11258966-A-G

110164355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259013-T-C

110164442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259095-T-C

110164486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259155-C-T

110164701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259346-T-C

http://identifiers.org/hco/13/GRCh38#110164768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11259415-C-A

110164768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259415-C-T

110164800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259446-G-A

110164800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259446-G-T

http://identifiers.org/hco/13/GRCh38#110164815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11259468-C-A

110164815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11259468-C-T

110164968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11259628-G-A

110164968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11259628-G-C

http://identifiers.org/hco/13/GRCh38#110166322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11260848-C-A

110166322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260848-C-T

110166336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260863-G-A

110166336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260863-G-T

110166358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260885-A-G

110166416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260928-T-C

110166497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260977-A-G

110166497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11260977-A-T

110166778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261216-C-T

110166880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261314-T-C

110166930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261373-A-G

http://identifiers.org/hco/13/GRCh38#110167010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11261454-C-A

110167010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261454-C-T

http://identifiers.org/hco/13/GRCh38#110167011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11261455-A-C

110167011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261455-A-T

110167012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261456-G-A

110167012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261456-G-C

110167012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261456-G-T

110167036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261483-G-T

110167104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261626-T-A

110167111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261651-G-T

110167132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261672-G-A

110167132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261672-G-T

110167317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261915-G-A

110167317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261915-G-T

110167345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261942-G-A

110167345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261942-G-C

110167345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11261942-G-T

110167488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262051-G-C

http://identifiers.org/hco/13/GRCh38#110167705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11262249-A-C

110169303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262341-T-C

110169347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262385-T-G

110169481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262487-G-A

110169481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262487-G-T

110169517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262508-C-T

110169529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262520-T-A

110169529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262520-T-C

110169743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11262716-C-T

110169784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262756-A-G

http://identifiers.org/hco/13/GRCh38#110169899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11262860-A-C

http://identifiers.org/hco/13/GRCh38#110169914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11262873-C-A

110169914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262873-C-T

110169962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262911-T-A

http://identifiers.org/hco/13/GRCh38#110169976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11262925-C-A

110169976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11262925-C-T

110170287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11263349-C-T

110170288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11263350-G-A

110170312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11263365-G-A

http://identifiers.org/hco/13/GRCh38#110170419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11263466-C-A

110170419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11263466-C-G

110170419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11263466-C-T

http://identifiers.org/hco/13/GRCh38#110170641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11263598-C-A

110170701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11263658-T-C

http://identifiers.org/hco/13/GRCh38#110170738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11263695-C-A

110170738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11263695-C-T

110170772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11263733-C-T

110172773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 11264705-A-G

110172865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11264786-C-T

110172897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11264818-T-C

110173483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266314-A-G

http://identifiers.org/hco/13/GRCh38#110173517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11266356-C-A

110173711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266548-C-T

http://identifiers.org/hco/13/GRCh38#110173712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11266549-C-A

http://identifiers.org/hco/13/GRCh38#110173771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11266593-A-C

110173771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266593-A-G

110173777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266599-T-C

110173783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266605-G-T

110173819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266628-A-G

110173835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266643-C-T

110173841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266647-G-T

110173858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266661-G-C

110173931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11266732-G-T

110173946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11266747-T-A

110173946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11266747-T-C

110173976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11266777-G-A

http://identifiers.org/hco/13/GRCh38#110174027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11266824-C-A

110174027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266824-C-G

110174027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266824-C-T

110174051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266847-G-A

110174051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266847-G-C

110174051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266847-G-T

110174077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266871-G-A

110174077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266871-G-T

110174122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266908-C-T

110174128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11266914-G-A

110174294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267072-C-G

110174399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267218-C-T

110174430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267247-A-G

110174559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267377-T-A

110174559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267377-T-C

110174579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267396-A-G

110174605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267416-G-A

110174642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11267453-G-A

110174642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11267453-G-C

http://identifiers.org/hco/13/GRCh38#110174732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11267543-C-A

110174732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11267543-C-T

110174767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267578-G-C

http://identifiers.org/hco/13/GRCh38#110174768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11267579-C-A

110174768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267579-C-T

110174769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267580-A-G

110174769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267580-A-T

110174868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267669-T-C

http://identifiers.org/hco/13/GRCh38#110175067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11267812-C-A

110175067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11267812-C-T

110175401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268093-G-T

110175495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268096-G-A

110175495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268096-G-T

110175744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268253-G-A

110175870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268358-G-A

110176265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268565-G-A

110176358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268611-T-C

110176393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268649-G-A

110176393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268649-G-T

110176613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268857-C-T

110176754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11268997-C-T

http://identifiers.org/hco/13/GRCh38#110176831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11269051-A-C

110177050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269245-G-C

110177057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269256-C-G

110177057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269256-C-T

http://identifiers.org/hco/13/GRCh38#110177179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11269360-C-A

110177179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269360-C-T

110177268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269430-C-T

110177273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269435-T-C

110177325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269476-T-C

110177325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269476-T-G

110177667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269820-T-C

110177743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269874-G-A

110177743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269874-G-C

110177743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269874-G-T

110177751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11269882-G-T

110177912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11270057-G-A

110177912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11270057-G-T

110177962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270106-T-G

110177991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270141-T-C

http://identifiers.org/hco/13/GRCh38#110178006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11270156-A-C

110178006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270156-A-G

110178107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11270252-G-A

110178107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: 11270252-G-C

http://identifiers.org/hco/13/GRCh38#110178188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11270333-A-C

http://identifiers.org/hco/13/GRCh38#110178280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11270411-A-C

110178645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270746-T-C

110178709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270799-T-C

110178709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270799-T-G

http://identifiers.org/hco/13/GRCh38#110178784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11270876-C-A

110178784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270876-C-T

110178849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270930-A-G

110178863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron variant
orthologous variants: 11270940-C-T

http://identifiers.org/hco/13/GRCh38#110178881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11270952-C-A

110178881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11270952-C-G

110178881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11270952-C-T

http://identifiers.org/hco/13/GRCh38#110178885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11270956-C-A

110178885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11270956-C-T

http://identifiers.org/hco/13/GRCh38#110178951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11271010-A-C

110178971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11271030-G-A

110179026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11271085-T-C

110179052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271109-T-C

110179068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271121-A-G

110179127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271179-G-A

110179127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271179-G-T

110179190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271227-A-G

110179198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271233-T-A

110179198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271233-T-C

110179213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271248-T-C

110179234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271270-T-A

110179266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271284-G-A

110179323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11271341-G-A

110179323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11271341-G-T

110180572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271623-G-A

110180572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271623-G-C

110180602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271652-G-A

110180602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271652-G-T

110180670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271711-T-C

http://identifiers.org/hco/13/GRCh38#110180740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11271791-C-A

http://identifiers.org/hco/13/GRCh38#110180762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11271796-C-A

110180762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271796-C-T

110180768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271802-T-A

110180798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271831-G-C

110180857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271869-C-T

110180957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11271955-T-C

110181165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272090-T-C

110181247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272155-C-G

110181247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272155-C-T

http://identifiers.org/hco/13/GRCh38#110181538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11272439-A-C

110181538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272439-A-G

110181579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272493-C-T

110181593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11272501-A-G

110183000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11273006-G-A

110183041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11273047-C-T

110183054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11273060-T-A

110183118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273124-A-T

110183135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273141-C-T

http://identifiers.org/hco/13/GRCh38#110183157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11273161-C-A

110183157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273161-C-T

110183305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273724-G-A

110183305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273724-G-C

110183305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273724-G-T

http://identifiers.org/hco/13/GRCh38#110183325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11273755-A-C

110183531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11273931-G-A

110183615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274013-G-A

110183616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274014-G-A

110183616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274014-G-T

110183661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274096-A-G

110183744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274178-C-T

110183780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274207-G-A

110183955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274351-A-T

110183956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274352-C-T

110184031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274422-G-A

110184211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274581-C-T

110184283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274643-T-A

110184297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274657-T-C

110184463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274773-C-T

110184466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274776-T-C

110184625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274911-G-A

110184851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11274976-C-T

110185059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275120-C-T

110185099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275123-C-T

110185102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275126-G-A

110185264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275313-G-A

110185289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275331-G-A

110185409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275438-G-A

http://identifiers.org/hco/13/GRCh38#110185427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11275487-A-C

110185466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275537-T-A

110185644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275731-T-C

110185908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275950-C-T

110185941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11275986-C-T

110186001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276034-G-A

110186093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276111-G-A

110186200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276180-T-C

110186243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276222-G-T

http://identifiers.org/hco/13/GRCh38#110186252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11276231-C-A

110186252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276231-C-T

110186269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276248-A-G

110186269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276248-A-T

110186407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11276347-G-A

http://identifiers.org/hco/13/GRCh38#110186518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11276458-A-C

110186518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11276458-A-G

110186521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11276461-G-A

http://identifiers.org/hco/13/GRCh38#110186580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11276520-C-A

110186580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276520-C-T

110186589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276527-A-G

110186745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11276625-T-C

110187171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11276983-G-C

110187171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11276983-G-T

110187219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11277031-T-C

110187641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11277401-C-G

110188212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11277891-G-A

110189397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278831-G-T

110189398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278832-G-C

http://identifiers.org/hco/13/GRCh38#110189435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11278871-C-A

110189435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278871-C-T

110189448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11278884-G-A

110189642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279015-G-A

110189647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279020-T-C

110189773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279143-G-A

110189827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279209-A-G

110189908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279283-C-T

110190165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279530-G-C

110190609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11279912-T-C

110190840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280091-T-C

110190851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280096-T-G

110190890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280136-T-C

110191204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280490-T-C

http://identifiers.org/hco/13/GRCh38#110191268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11280560-A-C

110191268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280560-A-G

110191432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280722-G-A

110191432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280722-G-C

110191432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280722-G-T

http://identifiers.org/hco/13/GRCh38#110191574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11280905-A-C

110191604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280935-A-G

110191611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11280951-T-C

110191692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281012-G-A

110191692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281012-G-T

110191838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281122-G-A

http://identifiers.org/hco/13/GRCh38#110192101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11281312-C-A

110192101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281312-C-T

110192181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281368-G-A

110192181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281368-G-C

110192181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281368-G-T

110192332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281503-C-T

110192349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281517-T-A

110192349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281517-T-C

110192380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281548-A-G

110192381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281549-G-A

110192381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281549-G-T

110192382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281550-G-A

110192382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281550-G-C

110192382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281550-G-T

110192395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281563-G-C

110192395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281563-G-T

110192467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281641-G-A

110192745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281866-C-T

110192749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281870-G-A

110192749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11281870-G-T

http://identifiers.org/hco/13/GRCh38#110192931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11282046-A-C

110192945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11282083-T-A

110192945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11282083-T-C

110192971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11282109-T-C

110193006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11282139-T-A

110193006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11282139-T-G

110193014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11282147-T-A

110194487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11283328-C-T

110194713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11283541-C-T

110194788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11283573-G-A

http://identifiers.org/hco/13/GRCh38#110194879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11283680-A-C

110194903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11283703-T-G

http://identifiers.org/hco/13/GRCh38#110194913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11283712-C-A

110195236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11284043-G-A

110195236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11284043-G-C

110195236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11284043-G-T

110197478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11284111-G-A

110197510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11284140-A-G

http://identifiers.org/hco/13/GRCh38#110197635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11284255-C-A

110197660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11284280-A-G

110197810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11284423-G-A

110198347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11284979-A-G

http://identifiers.org/hco/13/GRCh38#110198388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, stop_lost
orthologous variants: http://identifiers.org/mco/8/GRCm39#11285032-C-A

http://identifiers.org/hco/13/GRCh38#110198407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11285050-C-A

110198416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 11285059-A-G

110198647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11285276-A-G

110200807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286013-C-T

110200811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286017-A-G

110200913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286111-G-C

110201081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286274-G-A

http://identifiers.org/hco/13/GRCh38#110201391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11286391-A-C

110201391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286391-A-T

http://identifiers.org/hco/13/GRCh38#110201397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11286397-A-C

110201397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286397-A-G

110201397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286397-A-T

110201398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286398-G-A

110201398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286398-G-C

110201398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11286398-G-T

110201509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11286497-C-T

110203235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11287636-T-A

110203235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11287636-T-C

110203656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11287922-G-A

110203798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11288079-C-T

110203802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11288083-T-C

110204883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288361-G-A

110205007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288693-C-G

110205007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288693-C-T

110205036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288699-G-A

http://identifiers.org/hco/13/GRCh38#110205046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11288709-A-C

110205083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288739-T-C

110205181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288831-T-C

110205267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288915-A-T

110205330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11288979-C-T

110205542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11289182-T-C

http://identifiers.org/hco/13/GRCh38#110205559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11289199-C-A

110205559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289199-C-T

110206267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289489-G-A

http://identifiers.org/hco/13/GRCh38#110206558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11289720-C-A

http://identifiers.org/hco/13/GRCh38#110206606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11289763-C-A

110206606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289763-C-T

110206631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289788-G-A

110206631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289788-G-T

110206743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289908-T-C

110206743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289908-T-G

110206751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289916-C-T

110206782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289956-T-C

110206782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289956-T-G

http://identifiers.org/hco/13/GRCh38#110206810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11289984-C-A

110206810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11289984-C-T

http://identifiers.org/hco/13/GRCh38#110206826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11289996-C-A

110206947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290133-A-G

110206948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290135-T-A

110206948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290135-T-C

http://identifiers.org/hco/13/GRCh38#110206958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11290145-A-C

110206958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290145-A-G

http://identifiers.org/hco/13/GRCh38#110206959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11290146-A-C

http://identifiers.org/hco/13/GRCh38#110206963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11290150-A-C

110206963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290150-A-T

http://identifiers.org/hco/13/GRCh38#110206964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11290151-C-A

110206964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290151-C-G

110206964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290151-C-T

110206968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290155-A-G

110206968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11290155-A-T

110207285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291003-T-C

110207328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291046-A-G

110207328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291046-A-T

110207379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291097-T-C

110207379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291097-T-G

http://identifiers.org/hco/13/GRCh38#110207390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11291109-A-C

110207390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291109-A-G

110207463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11291182-T-A

110207463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11291182-T-G

http://identifiers.org/hco/13/GRCh38#110207567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11291276-A-C

110207567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291276-A-T

110207774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291415-C-G

110207774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291415-C-T

110207788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291429-G-A

110208483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11291948-G-A

110208600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292058-T-C

110208613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292073-G-A

110208613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292073-G-C

110208906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292230-T-C

110208937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292257-T-C

110208937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292257-T-G

110208943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292259-G-A

110208977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292291-A-T

110208980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292294-G-A

110208980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292294-G-T

110208985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292299-T-C

110208986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292300-T-A

110209008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292322-T-A

110209008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292322-T-C

110209008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292322-T-G

110209062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292368-G-A

110209062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292368-G-T

110209078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292391-T-G

110209345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292734-T-C

110209345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292734-T-G

110209356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292745-T-C

110209440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292830-G-A

110209440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11292830-G-T

110209970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11294331-C-T

110210010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11294371-A-G

110210045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11294407-A-G

110210046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11294408-G-C

110210121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11294477-A-G

110210180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11294537-G-A

110210186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11294543-A-G

110210186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 11294543-A-T

110210271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11294628-T-A

110210271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11294628-T-C

110210314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11294658-A-G

110210325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11294669-G-A

110210325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11294669-G-T

110210328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11294672-A-G

110211626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295037-G-A

http://identifiers.org/hco/13/GRCh38#110211908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11295250-C-A

110211908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11295250-C-G

110211908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11295250-C-T

110212010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11295335-T-C

http://identifiers.org/hco/13/GRCh38#110212012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11295337-C-A

110212167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11295490-G-C

110212277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11295642-A-T

110212399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11295721-T-G

110212459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11295779-G-A

http://identifiers.org/hco/13/GRCh38#110212554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11295873-A-C

110212554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295873-A-G

110212559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295878-G-A

110212559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295878-G-C

110212638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295956-A-G

110212649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295966-G-T

110212652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295969-G-A

110212652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295969-G-C

http://identifiers.org/hco/13/GRCh38#110212667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11295984-A-C

110212667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11295984-A-T

http://identifiers.org/hco/13/GRCh38#110212733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11296025-C-A

110212733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296025-C-G

110212733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296025-C-T

110213479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296616-T-C

http://identifiers.org/hco/13/GRCh38#110213682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11296759-A-C

110213682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296759-A-G

110213682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296759-A-T

110213755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296826-T-C

110213849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296930-T-C

110213867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296950-A-T

110213882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296964-G-A

110213882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296964-G-C

110213882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296964-G-T

110213906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11296988-A-T

110213971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 11297051-A-G

110214054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11297119-T-A

110214982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298037-T-A

110214982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298037-T-C

110215026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298083-T-C

110215146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298189-A-G

110215742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11298862-T-G

110216234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299242-A-G

110216261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299265-C-T

110216279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299295-T-C

110216279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299295-T-G

110216456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299476-G-A

http://identifiers.org/hco/13/GRCh38#110216472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11299492-C-A

110216472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299492-C-G

110216935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299951-C-T

110216967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11299983-G-A

110217181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300189-G-A

110217226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300237-G-T

110217515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300502-T-C

110217619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300663-C-T

110217643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300687-A-T

110217657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11300808-G-C

110217727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301007-C-T

110217769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301045-C-T

110217855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301131-T-A

110217938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301206-G-A

110217965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301233-C-G

110217965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301233-C-T

110218095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11301335-A-G

110218422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302047-C-G

110218633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302222-C-T

110218666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302233-G-A

110218666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302233-G-C

110218914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302478-G-C

110219112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302697-G-A

110221213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11302948-G-A

110221408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303122-G-A

http://identifiers.org/hco/13/GRCh38#110221483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11303189-C-A

110221483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11303189-C-T

110223302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304329-T-A

110223302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11304329-T-C

http://identifiers.org/hco/13/GRCh38#110223456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11304530-C-A

http://identifiers.org/hco/13/GRCh38#110223672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11304855-A-C

http://identifiers.org/hco/13/GRCh38#110223812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11305092-C-A

110223813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305093-C-G

110223912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305212-T-C

110224016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305318-A-G

110224098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305391-T-C

http://identifiers.org/hco/13/GRCh38#110224299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11305582-C-A

110224304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11305587-T-C

110226705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11306774-A-G

110226857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11306929-G-A

110226857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11306929-G-C

110226949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11306992-C-G

110227457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307450-G-A

110227466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307459-G-A

110227466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11307459-G-T

110228652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308311-T-C

http://identifiers.org/hco/13/GRCh38#110228948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11308547-C-A

110228948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308547-C-T

110228977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308567-A-G

110229050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11308629-G-C

http://identifiers.org/hco/13/GRCh38#110229319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11308856-C-A

110229582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309035-C-T

110229610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309076-T-C

110229677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309134-G-A

110229693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11309167-T-C

110231563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310401-T-G

110231674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310504-G-A

110232101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11310934-T-A

http://identifiers.org/hco/13/GRCh38#110232293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11311345-A-C

110232401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311450-C-T

110232561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311596-A-G

110232693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311734-C-T

110232710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11311751-T-G

110233027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312167-G-C

110233087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312225-T-C

110233264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312386-T-A

110233416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312524-G-A

110233505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312622-T-C

110233520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312637-T-C

110233526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312642-G-C

110233666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312790-T-A

110233734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312852-G-A

110233734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312852-G-T

110233814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11312919-T-C

http://identifiers.org/hco/13/GRCh38#110233820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11312923-C-A

110233949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11313009-G-A

110236970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11314730-T-C

110236999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11314757-C-T

110237082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11314829-C-G

110237086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11314833-C-T

110237339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11314948-G-T

110237424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11315010-T-C

110237474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 11315057-G-A

http://identifiers.org/hco/13/GRCh38#110237869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11315435-A-C

110237903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315473-A-G

110237932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315501-G-A

110238014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315582-C-G

110238073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315611-T-A

110238073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315611-T-C

110238234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11315775-A-G

110238742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316074-C-T

http://identifiers.org/hco/13/GRCh38#110239508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11316787-A-C

110239508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11316787-A-G

http://identifiers.org/hco/13/GRCh38#110242355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11317286-A-C

110242365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11317296-C-T

110242553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11317483-G-T

110242591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11317519-T-C

110242665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 11317587-G-A

110242752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317676-C-T

http://identifiers.org/hco/13/GRCh38#110242755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11317679-C-A

110242755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11317679-C-G

110243891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318533-T-C

110244359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11318989-G-A

110244405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319033-A-G

110244616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319215-C-T

http://identifiers.org/hco/13/GRCh38#110244722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11319256-C-A

110244722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319256-C-T

110244834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319342-C-T

110244882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319390-T-C

110245266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319463-C-T

110245284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319481-G-A

110245286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319483-G-C

110245583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319731-G-C

110245701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319844-G-A

110245790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319915-G-T

110245806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319927-A-G

110245814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11319934-C-T

110245962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320053-T-A

110246537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320784-T-A

110246537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320784-T-C

110246558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320811-T-A

110246561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320814-A-T

110246697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320930-G-C

110246711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11320951-A-G

110246859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11321072-G-T

110246914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11321108-G-A

110246952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11321143-G-A

http://identifiers.org/hco/13/GRCh38#110246967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11321159-A-C

110247420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11321944-G-C

110247532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322053-A-G

110247573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322082-A-T

http://identifiers.org/hco/13/GRCh38#110248075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11322459-C-A

110248210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322592-C-T

110248247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11322629-C-G

110250026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323272-T-C

110250164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323406-G-A

110250241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323481-G-C

110250594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11323839-T-C

110250756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11323982-C-T

110254456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11324761-A-G

110254564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11324868-T-C

http://identifiers.org/hco/13/GRCh38#110254596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11324886-A-C

110254696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11324980-G-A

110255974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325049-C-T

110256044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325129-G-T

110256888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325846-G-A

110256888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325846-G-T

110256922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11325880-C-T

110257377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326278-C-T

110257505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326417-A-G

110257572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326486-A-G

110257763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326642-A-G

110257779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326658-A-G

110257963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326871-C-G

110257971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326879-C-T

110258006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11326931-G-A

110261120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327661-G-T

110261133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327687-A-G

110261134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327688-T-C

110261195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327749-G-A

110261216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327770-G-A

110261263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327843-C-G

110261264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327844-C-G

110261338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327915-G-T

110261417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11327975-G-A

110261744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11328312-C-T

110262118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11328649-T-C

110262663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11329399-A-G

110262664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11329400-G-T

110262669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11329405-T-C

110262948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11329665-T-C

110263189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11329893-G-A

110263305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330000-A-G

110263448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330140-C-T

110263475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330154-A-G

110263599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330178-G-A

110263627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330200-T-G

110263679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330251-G-T

http://identifiers.org/hco/13/GRCh38#110264145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11330666-A-C

110264179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330698-G-A

110264737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11330980-C-T

110264827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331027-T-C

110265095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331317-G-A

110265148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331380-G-A

110265148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331380-G-T

110265150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331381-G-A

110265152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331383-G-T

110265160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331391-A-T

110265211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11331425-G-T

110265288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331504-C-T

http://identifiers.org/hco/13/GRCh38#110265380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11331582-A-C

110265380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331582-A-G

110265408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331611-G-A

110265408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331611-G-T

110265569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331759-A-G

110265637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331802-G-T

110265671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331839-T-C

110265685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331870-G-C

110265731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331900-T-A

110265731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331900-T-C

110265753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331921-A-G

110265775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331943-C-G

110265775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331943-C-T

110265818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11331984-G-T

110265883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11332043-T-G

110265942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11332101-T-A

110265956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11332111-G-T

110265979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11332134-G-A

http://identifiers.org/hco/13/GRCh38#110266085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11332241-C-A

110266085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11332241-C-T

http://identifiers.org/hco/13/GRCh38#110266103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11332259-C-A

110266103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 11332259-C-T

110266154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332300-C-T

http://identifiers.org/hco/13/GRCh38#110266250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11332396-C-A

110266250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332396-C-T

110266336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332475-C-T

110266561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332643-G-C

110266601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332688-C-T

110266627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332710-G-C

110266627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11332710-G-T

110267214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11333501-G-A

110267313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11333595-C-T

110267605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11333878-G-A

110270132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334305-T-A

110270153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334325-G-A

110270183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334380-A-G

110270196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334406-T-C

110270323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11334533-C-T

110273624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335488-T-A

http://identifiers.org/hco/13/GRCh38#110273678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11335544-C-A

110273753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11335622-G-A

110277152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338031-A-G

110277211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338090-G-C

110277301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338172-T-C

http://identifiers.org/hco/13/GRCh38#110277392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11338264-C-A

110277986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338704-C-G

110278139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11338930-T-C

110278531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339326-C-T

110278888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339681-A-T

110278986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11339853-A-G

110279183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340052-C-T

110279414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340254-G-A

110279546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340372-G-C

110279546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340372-G-T

110279547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340373-G-A

110279547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340373-G-C

110279598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340420-T-A

110279598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340420-T-G

110279673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340495-G-A

110279707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340529-C-T

110279764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340588-C-G

110279764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340588-C-T

110279863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340675-A-G

110279863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340675-A-T

110279938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340735-C-T

110279941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340738-C-T

http://identifiers.org/hco/13/GRCh38#110280163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11340973-A-C

110280163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11340973-A-G

110280269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341068-G-A

110280297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341100-A-T

110280464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341268-T-C

110280499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341303-G-A

http://identifiers.org/hco/13/GRCh38#110280520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11341324-A-C

110280520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341324-A-G

110280581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341384-G-A

110280581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341384-G-T

110280991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11341747-T-C

110281140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11342761-T-G

110281171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11342791-C-T

110281264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11342874-C-G

110284427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345256-G-T

110285449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11345707-A-G

110285811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346023-T-C

http://identifiers.org/hco/13/GRCh38#110285826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11346039-C-A

110285826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346039-C-T

110285872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346062-T-C

110285903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346073-T-G

110286057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346214-T-C

110286109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346264-G-A

110286164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346302-C-T

110286342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346451-T-G

110286400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346512-G-T

110286467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346601-G-A

110286592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346722-G-A

110286592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346722-G-T

110286661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11346788-G-A

110287368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347415-T-C

110287574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347581-G-A

110287756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11347754-G-C

110289910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11348811-G-A

110289910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11348811-G-C

110290067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349006-T-G

110290319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349273-A-G

110290430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11349384-T-C

110293937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11350633-G-A

110294338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11350973-C-T

110294430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351030-T-C

110294591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351181-C-G

110294733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351322-G-A

http://identifiers.org/hco/13/GRCh38#110294937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11351504-C-A

110294967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351544-T-C

110295032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11351608-A-G

110298114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353754-T-A

110298144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353784-T-A

http://identifiers.org/hco/13/GRCh38#110298267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11353947-C-A

110298277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11353961-T-C

110298387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11354067-T-G

110298506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11354170-T-C

110298691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 11354388-G-A

110298980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11354588-A-G

110299146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11354717-G-C

http://identifiers.org/hco/13/GRCh38#110299260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11354874-A-C

110299411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355020-G-A

110299414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355023-G-A

http://identifiers.org/hco/13/GRCh38#110299416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11355026-C-A

110299693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355264-T-C

110299738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355309-T-A

110299830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11355593-G-C

110300704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11357102-G-A

110300794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11357170-A-G

http://identifiers.org/hco/13/GRCh38#110301025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11357373-A-C

http://identifiers.org/hco/13/GRCh38#110301302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11357686-C-A

110301302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11357686-C-T

110301819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358104-G-A

110301819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358104-G-C

110302203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358335-C-G

110302266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358369-G-A

110302293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358406-C-T

110302326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358430-A-G

110302402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358482-T-C

110302412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358492-G-A

110302412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358492-G-T

110302706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11358747-A-G

http://identifiers.org/hco/13/GRCh38#110302971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11359017-A-C

110303218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11359260-G-A

110303314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11359357-G-A

110303326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11359369-A-G

110303793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11359749-G-A

http://identifiers.org/hco/13/GRCh38#110303912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11359875-C-A

110304085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360012-T-A

110304085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360012-T-C

110304316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11360225-G-C

http://identifiers.org/hco/13/GRCh38#110305790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#11361445-C-A

110305943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 11361585-G-T

110306055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361695-G-C

110306055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361695-G-T

110306058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361698-G-C

110306073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361711-G-A

110306207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11361822-T-C

110306633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362209-G-A

110306633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362209-G-C

http://identifiers.org/hco/13/GRCh38#110306856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#11362421-C-A

110306856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362421-C-T

110306868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362437-G-A

110306868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 11362437-G-T

110306930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 11362502-G-T

110307073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362665-G-A

110307073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362665-G-T

110307077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362669-G-A

110307077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2202
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 11362669-G-T