92883597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12983490-A-T

92883740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12983359-G-A

92884180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12982955-T-C

92884288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12982858-G-A

92884658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12982496-G-T

92885278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12981876-T-A

92885278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12981876-T-C

92885305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12981850-G-T

92885556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12981557-T-A

92885597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12981525-A-T

http://identifiers.org/hco/8/GRCh38#92885627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12981500-C-A

92885751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12981382-G-C

http://identifiers.org/hco/8/GRCh38#92885974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12981163-C-A

92886110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12981029-T-C

92886124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12981015-G-A

92886268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12980865-T-A

92886301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12980833-A-G

92886338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12980797-T-C

92886404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12980736-G-T

http://identifiers.org/hco/8/GRCh38#92886471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12980671-C-A

92886471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12980671-C-T

92886472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12980670-A-G

92886664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 12980474-G-A

92886767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980372-G-A

92886767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980372-G-T

92886778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980361-A-T

92886829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980319-G-A

92886829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980319-G-C

92886829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980319-G-T

92886833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980315-A-G

92886961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980211-T-A

92887005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980185-T-C

92887178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12980014-T-A

92887498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12979353-A-G

92887636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12979232-T-G

92888079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12978789-C-T

92888106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12978762-C-G

92888749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12978143-G-C

92888840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12978053-T-C

92889036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977571-C-T

92889061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977547-T-G

92889092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977517-T-C

92889294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977330-T-C

http://identifiers.org/hco/8/GRCh38#92889505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12977127-A-C

92889522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977110-A-G

92889548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977083-G-A

92889548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977083-G-T

92889557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12977074-T-C

92889683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976964-C-T

92889824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976821-G-C

92889888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976757-A-G

92889976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976699-T-C

92889986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976694-C-T

92890026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976654-A-G

92890279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976407-C-T

92890385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976325-T-A

92890703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12976039-T-C

92890894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12975871-A-G

92891697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12975137-T-C

92891738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12975096-G-C

92891854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974968-A-T

92891881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974941-T-A

92891881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974941-T-C

92891881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974941-T-G

92891890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974933-G-T

http://identifiers.org/hco/8/GRCh38#92891921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12974890-C-A

92891921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974890-C-T

92891968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974834-A-G

92892126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974675-T-A

92892126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974675-T-C

http://identifiers.org/hco/8/GRCh38#92892198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12974602-C-A

92892198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974602-C-T

92892404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974421-G-A

92892405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12974420-T-C

92893058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973844-T-C

92893402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973489-T-C

92893606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973273-A-G

92893724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973160-G-A

92893781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973110-A-G

92893781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973110-A-T

92893859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12973047-G-A

92907776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12971511-C-T

92908039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12971258-G-A

92908039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12971258-G-C

92908247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12971065-C-T

92908894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12970430-T-C

92909348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12970005-G-A

92909402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969956-C-T

92909458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969905-A-G

92909567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969805-C-T

92909639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969739-A-G

92909651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969727-G-A

92909695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969675-T-C

92910185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969164-T-C

92910185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969164-T-G

92910189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969160-T-C

92910195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969155-T-C

92910351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969014-A-G

92910355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969010-A-T

92910359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969006-G-A

92910359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969006-G-T

92910360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12969005-A-G

92910403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12968962-G-A

92910614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12968740-G-T

92910638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12968716-A-T

http://identifiers.org/hco/8/GRCh38#92910945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12968447-A-C

92910945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12968447-A-G

92911587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12967873-A-T

92911596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12967825-A-G

92916132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963759-T-C

92916316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963588-C-T

92916365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963538-T-C

92916642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963290-T-C

92916665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963271-G-T

92916740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963197-A-G

92916766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963168-C-T

92916806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963131-G-T

92916832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963103-G-A

92916832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963103-G-T

92916835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963100-T-A

http://identifiers.org/hco/8/GRCh38#92916846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12963089-A-C

92916846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963089-A-G

92916856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963079-T-C

92916872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963064-A-G

92916872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963064-A-T

92916885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963051-T-A

92916885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12963051-T-C

http://identifiers.org/hco/8/GRCh38#92917035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12962911-A-C

92917065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12962883-T-C

92922064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12960528-A-T

92922116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12960474-T-C

92922247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12960340-G-A

92922456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12960146-A-G

92922456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12960146-A-T

92922469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12960131-T-A

http://identifiers.org/hco/8/GRCh38#92923334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12952768-A-C

92923440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12952662-T-C

92927671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948597-T-C

92927785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948471-G-A

92927799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948457-T-A

http://identifiers.org/hco/8/GRCh38#92927801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12948455-C-A

92927820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948436-A-G

92927960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12948302-T-C

92928082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948145-A-G

92928166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948036-T-A

92928173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12948029-C-T

92928296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947907-T-G

92928508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947713-C-T

92928555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947666-T-A

92928886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947241-A-G

92928912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947215-G-A

92928935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947196-T-C

92928982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947150-C-T

92929044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947088-G-C

92929049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12947084-A-G

http://identifiers.org/hco/8/GRCh38#92929131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12947016-C-A

92929224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946927-G-T

92929236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946923-A-T

92929255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946908-T-C

92929267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946896-T-A

92929267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946896-T-C

92929368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946795-A-G

92929578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12946615-G-A

92929631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946562-G-A

92929631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946562-G-T

92929698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12946496-T-C

http://identifiers.org/hco/8/GRCh38#92930448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12945349-C-A

92930477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12945325-T-C

http://identifiers.org/hco/8/GRCh38#92930757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12944688-A-C

92930850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12944600-T-A

92930850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12944600-T-C

92930888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12944546-G-A

92930945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12944488-T-C

92933800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12933833-T-C

http://identifiers.org/hco/8/GRCh38#92933821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12933812-A-C

92933975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12933678-A-T

92934139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12933532-G-T

92934600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12933104-T-C

92934728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12932970-T-C

92935336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12932422-G-T

92945875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926772-G-T

92946143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926573-C-G

92946145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926571-G-C

http://identifiers.org/hco/8/GRCh38#92946254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12926463-A-C

92946256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926461-A-G

http://identifiers.org/hco/8/GRCh38#92946532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12926166-A-C

92946536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926162-C-T

92946545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926153-A-G

92946555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926144-A-G

http://identifiers.org/hco/8/GRCh38#92946634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12926057-A-C

92946656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926039-A-T

92947145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925900-C-T

92947628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924809-T-C

92947658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924776-T-C

92947715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924719-A-G

92947719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924715-C-T

92947828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924613-G-A

92952808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919618-T-C

92952820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919606-C-T

92952831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919595-G-C

92952831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919595-G-T

92952842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919584-C-T

http://identifiers.org/hco/8/GRCh38#92952937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12919492-A-C

92952937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919492-A-G

92952998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919416-T-C

92953310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919090-G-A

92953337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919051-A-G

92953338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919050-A-G

92953404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12918977-G-A

92953519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918874-A-T

92953524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918869-A-G

92953524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918869-A-T

92953628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918771-G-A

92953654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918746-A-T

92953655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918745-A-G

92953836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918603-G-A

92953918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918522-T-C

92954136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12918327-G-A

92954908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916760-G-A

92954908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916760-G-T

92954935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916734-C-G

92955113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916561-G-A

92955114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916560-T-C

92955126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916541-C-T

http://identifiers.org/hco/8/GRCh38#92955369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12916062-A-C

92955458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915966-A-G

92955685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915788-G-T

92955980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915508-C-T

92956142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915335-T-C

92956662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914939-C-G

92956778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914831-T-C

92956972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914633-C-T

92957085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914516-C-G

http://identifiers.org/hco/8/GRCh38#92957186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12914434-C-A

92957642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914186-A-T

http://identifiers.org/hco/8/GRCh38#92957832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12913985-A-C

92957980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913832-A-G

92958125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913705-G-T

http://identifiers.org/hco/8/GRCh38#92958325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12913509-A-C

92958703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913161-G-T

92960649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12912480-C-T

92960662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12912467-G-T

92960685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12912444-G-T

92960752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912379-T-A

92960752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912379-T-C

92960785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912347-G-A

92960807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912329-G-A

92960807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912329-G-T

92960925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912250-T-G

92960964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912210-C-G

92960972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912199-C-T

92960987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912184-T-C

92961040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912135-T-C

92961899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911521-C-T

92962170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911299-G-A

92962638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910898-A-G

92962659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910877-G-A

92962666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12910870-C-T

92963208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12909448-T-C

92963247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12909408-C-T

92963259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12909396-T-C

92963887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908824-C-T

92963953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908727-T-C

92963974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908707-A-G

92964073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908631-T-A

92964073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908631-T-G

92964101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908607-A-G

92964113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908580-G-A

92964206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908518-C-G

92964208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908516-G-A

92964288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908470-T-A

92964288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908470-T-C

92964345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908405-C-T

http://identifiers.org/hco/8/GRCh38#92964396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12908359-C-A

92964440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908317-A-G

http://identifiers.org/hco/8/GRCh38#92964468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12908283-A-C

92964468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908283-A-G

92964630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908122-G-A

92964927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907903-G-T

92964974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907857-A-G

92965261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907609-G-A

92965270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907605-T-C

92965320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907567-C-T

http://identifiers.org/hco/8/GRCh38#92965431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12907484-C-A

92965481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907437-A-G

http://identifiers.org/hco/8/GRCh38#92965505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12907412-C-A

92965505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12907412-C-G

92965505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12907412-C-T

92965548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12907364-G-A

92965548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12907364-G-T

92965596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12907314-G-A

92965596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12907314-G-T

92965645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907263-T-A

92965645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907263-T-G

92965672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907239-A-T

http://identifiers.org/hco/8/GRCh38#92965693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#12907221-C-A

92965693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907221-C-G

http://identifiers.org/hco/8/GRCh38#92965752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#12907171-C-A

92965881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907054-A-G

http://identifiers.org/hco/8/GRCh38#92965908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12907027-C-A

92965931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12907006-C-T

92965994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12906949-G-A

92966106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12906839-C-T

92966122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12906823-C-T

92966127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12906818-G-A

92966127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12906818-G-T

92966212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12906759-G-A

http://identifiers.org/hco/8/GRCh38#92966219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12906752-C-A

92966409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron_variant, undefined
orthologous variants: 12906582-C-T

92966639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12906365-G-A

92966687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12906315-A-G

92966708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12906294-T-C

92967166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12905492-T-C

http://identifiers.org/hco/8/GRCh38#92967320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12905421-C-A

92967368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12905373-T-A

93011853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890855-G-T

93011941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890781-G-A

93011956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890762-A-T

93012054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890669-C-T

93012139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890596-T-C

93012144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890591-G-C

93012152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890583-T-C

93012153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890582-G-A

93012240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890496-T-G

http://identifiers.org/hco/8/GRCh38#93012327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12890409-C-A

93012343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890393-G-A

93012358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890388-C-T

93012546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890193-G-T

93012574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890165-T-C

93012574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890165-T-G

93012592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890142-C-T

93012603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890131-T-G

http://identifiers.org/hco/8/GRCh38#93012640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12890094-C-A

93012658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890074-C-G

93012658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890074-C-T

93012668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890064-C-T

93012695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890042-A-G

93012714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12890019-A-G

93012755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12889964-C-G

93012867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12889863-A-T

93013056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12889628-T-G

93013144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12889551-G-A

93013241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12889461-G-A

93013479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12889171-G-A

93013711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12888940-G-C

93013991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12888656-G-A

93014534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12888134-G-A

93014761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12887906-T-G

93015109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12887557-A-T

93015319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12887388-T-A

93015319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12887388-T-C

93015455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12887265-A-G

93015641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12887098-A-T

93015849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886889-A-G

93015857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886881-G-A

93015869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886869-T-A

http://identifiers.org/hco/8/GRCh38#93015878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12886860-C-A

93015982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886744-T-C

http://identifiers.org/hco/8/GRCh38#93016141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12886592-A-C

93016180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886554-A-G

93016204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886530-C-T

93016330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886417-G-C

93016339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886408-A-G

93016349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886398-A-T

93016515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886280-T-C

93016558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886239-G-T

93016717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886088-A-G

93016778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886033-C-T

93016779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886032-A-G

93016788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12886023-G-A

93017064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885757-T-G

93017184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885723-T-G

http://identifiers.org/hco/8/GRCh38#93017202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#12885707-C-A

93017202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885707-C-T

93017210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885700-C-T

93017372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885571-G-A

93017426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885519-A-T

93017460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885496-A-G

93017460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: intron variant
orthologous variants: 12885496-A-T

93017639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27828
most severe consequence: 5 prime UTR variant
orthologous variants: 12885327-A-G