104937340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738686-A-G

104937345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738691-G-A

104937345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738691-G-T

104937416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738762-G-T

104937463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738812-G-A

104937463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738812-G-T

104937539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738889-G-A

104937571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112738920-T-A

104937755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739070-T-G

104937779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739094-T-C

104937879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739160-G-A

104937879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739160-G-T

104937997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739273-G-A

104938048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739323-G-A

104938056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 112739328-A-G

104938123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112739391-C-T

104938158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112739426-T-A

104938158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112739426-T-C

104938175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112739443-T-C

104938176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112739444-C-T

104938243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112739508-G-A

104938282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112739547-T-C

104938657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112739901-C-T

104938722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112739936-T-C

104938722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112739936-T-G

104938786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112740000-G-A

104938831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112740045-T-C

104938836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112740050-T-A

104939044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112740255-A-G

104939398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112740600-A-G

104939468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112740673-G-A

104939468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112740673-G-T

104939564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112740757-T-A

http://identifiers.org/hco/14/GRCh38#104939611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112740804-C-A

104939629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112740822-G-A

104939789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112740997-G-A

104939858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741072-G-A

104939858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741072-G-C

104939858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741072-G-T

104939978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741201-G-A

104939978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741201-G-T

104940032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741255-T-C

104940087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741304-G-A

104940093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112741310-G-A

104940093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741310-G-C

104940270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741427-T-G

104940325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741482-C-G

104940333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741490-G-C

http://identifiers.org/hco/14/GRCh38#104940406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112741563-C-A

http://identifiers.org/hco/14/GRCh38#104940449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112741607-A-C

104940839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112741990-A-G

104940871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742022-T-A

104940871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742022-T-C

104940946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742064-C-T

104940968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742078-G-T

104940971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742081-C-G

104940981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 112742091-T-C

104940981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 112742091-T-G

104941010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742128-G-A

104941042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742162-G-A

104941043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742163-G-A

http://identifiers.org/hco/14/GRCh38#104941057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742180-A-C

104941087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742194-C-T

104941099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742206-G-A

104941099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742206-G-C

104941115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742224-A-G

104941528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742619-C-T

http://identifiers.org/hco/14/GRCh38#104941703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742260-A-C

104941703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742260-A-G

104941705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742262-C-G

104941705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742262-C-T

http://identifiers.org/hco/14/GRCh38#104941707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742264-C-A

104941707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742264-C-T

104941711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742268-T-C

http://identifiers.org/hco/14/GRCh38#104941722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742279-C-A

104941728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742285-G-A

104941728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742285-G-C

104941735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742292-C-G

104941737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742294-T-C

http://identifiers.org/hco/14/GRCh38#104941742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742299-C-A

104941742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742299-C-T

104941743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742300-C-G

104941743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742300-C-T

104941747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742304-G-A

http://identifiers.org/hco/14/GRCh38#104941835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742428-A-C

104941835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742428-A-T

http://identifiers.org/hco/14/GRCh38#104941878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742990-C-A

104941902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743014-A-G

104941904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743016-G-A

104941984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112743096-A-G

http://identifiers.org/hco/14/GRCh38#104942023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742619-C-A

104942023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112742619-C-T

http://identifiers.org/hco/14/GRCh38#104942080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742676-A-C

104942103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742699-A-G

http://identifiers.org/hco/14/GRCh38#104942104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742700-C-A

http://identifiers.org/hco/14/GRCh38#104943192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112742783-C-A

104943192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742783-C-T

104943204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742795-G-A

104943204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112742795-G-C

104943439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112743066-G-A

104943439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112743066-G-C

http://identifiers.org/hco/14/GRCh38#104943565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112743195-C-A

104943565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112743195-C-T

104943687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743302-C-T

104943699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743314-G-A

104943699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743314-G-T

http://identifiers.org/hco/14/GRCh38#104944182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112743821-C-A

104944182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743821-C-G

104944182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743821-C-T

http://identifiers.org/hco/14/GRCh38#104944194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112743833-A-C

104944194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743833-A-G

104944194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112743833-A-T

104944954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112744653-A-G

104945035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112744737-C-T

104945068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112744770-C-T

104945073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112744775-A-G

104945073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112744775-A-T

http://identifiers.org/hco/14/GRCh38#104945172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112744859-C-A

104945172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112744859-C-T

104945449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112745172-A-T

http://identifiers.org/hco/14/GRCh38#104945545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746825-A-C

104945545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746825-A-T

http://identifiers.org/hco/14/GRCh38#104945667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746932-C-A

104945667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746932-C-G

104945667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746932-C-T

104945679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746944-G-C

104945679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746944-G-T

104945713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746978-T-C

104945722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746987-G-A

104945722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746987-G-T

104945778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747043-G-A

104945778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747043-G-T

104945800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747101-G-A

104945800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747101-G-C

http://identifiers.org/hco/14/GRCh38#104945935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112747236-C-A

104945935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747236-C-T

104945992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747296-G-A

104945992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747296-G-T

http://identifiers.org/hco/14/GRCh38#104946040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112747344-A-C

104946040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747344-A-G

104946040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747344-A-T

http://identifiers.org/hco/14/GRCh38#104946162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112747451-C-A

104946162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747451-C-G

104946162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747451-C-T

104946208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747497-T-A

104946217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747506-T-A

104946217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747506-T-C

104946217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747506-T-G

104946273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747562-G-T

104946295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747620-G-A

104946295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747620-G-C

104946333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747658-C-T

http://identifiers.org/hco/14/GRCh38#104946439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112747764-A-C

104946473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745209-G-A

http://identifiers.org/hco/14/GRCh38#104946535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112745271-A-C

104946535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112745271-A-G

104946535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112745271-A-T

104946657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745378-C-G

104946657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745378-C-T

104946669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745390-G-C

104946904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748253-G-A

104946904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748253-G-T

104946982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748334-G-A

104946982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748334-G-C

104947097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748434-G-A

104947141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-A

104947141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-C

http://identifiers.org/hco/14/GRCh38#104947152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-A

104947152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

104947180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-A

104947180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -G-C

104947197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

104947221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-G

104947221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

104947257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745527-G-A

104947257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745527-G-T

104947285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-A

104947285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-C

http://identifiers.org/hco/14/GRCh38#104947297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-A

104947297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-G

104947297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -C-T

104947424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8986277-A-G

104947525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8986193-T-A

104947525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8986193-T-C

http://identifiers.org/hco/14/GRCh38#104947647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8986072-C-A

104947647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8986072-C-G

104947647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8986072-C-T

104947659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8986060-G-A

104947924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746207-A-G

104948020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746306-A-G

104948020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746306-A-T

http://identifiers.org/hco/14/GRCh38#104948142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746413-C-A

104948142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746413-C-G

104948142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746413-C-T

http://identifiers.org/hco/14/GRCh38#104948515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112745790-A-C

104948515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112745790-A-T

http://identifiers.org/hco/14/GRCh38#104948637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112745897-C-A

104948637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745897-C-G

104948637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112745897-C-T

104948884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746177-G-A

104948884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746177-G-T

http://identifiers.org/hco/14/GRCh38#104948962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746258-A-C

104948962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746258-A-G

104948962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746258-A-T

104949077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746358-G-T

104949121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746402-G-A

104949121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746402-G-C

104949121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746402-G-T

104949132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746413-T-A

104949132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746413-T-C

104949132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746413-T-G

104949160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746441-T-A

104949160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746441-T-C

104949160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746441-T-G

http://identifiers.org/hco/14/GRCh38#104949177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746458-C-A

104949177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746458-C-T

104949201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746482-C-T

104949265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746582-G-A

104949265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746582-G-C

104949265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746582-G-T

104949277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746594-C-G

104949277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746594-C-T

http://identifiers.org/hco/14/GRCh38#104949393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746710-C-A

104949393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746710-C-T

104949404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746721-G-A

104949404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746721-G-C

104949409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746726-A-T

http://identifiers.org/hco/14/GRCh38#104949505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112748382-A-C

104949505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748382-A-T

104949904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8984073-A-G

http://identifiers.org/hco/14/GRCh38#104950000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112746825-A-C

104950000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746825-A-G

104950000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112746825-A-T

104950122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746932-C-T

104950134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746944-G-A

104950134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746944-G-T

104950399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747245-A-G

104950399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747245-A-T

104950495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747344-A-G

104950495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747344-A-T

104950629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747463-G-T

104950765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748154-T-A

104950765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748154-T-C

http://identifiers.org/hco/14/GRCh38#104950990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112748382-A-C

104950990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748382-A-G

104950990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748382-A-T

http://identifiers.org/hco/14/GRCh38#104951112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-A

104951112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-G

104951112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

104951124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -G-A

104951124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -G-C

104951300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746637-T-A

104951300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112746637-T-G

104951884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747764-A-G

http://identifiers.org/hco/14/GRCh38#104951980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112747863-A-C

104951980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747863-A-G

104951980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112747863-A-T

http://identifiers.org/hco/14/GRCh38#104952475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112748382-A-C

104952475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748382-A-G

104952475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748382-A-T

http://identifiers.org/hco/14/GRCh38#104952597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112747970-C-A

104952597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747970-C-G

104952597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112747970-C-T

104952708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748081-G-A

http://identifiers.org/hco/14/GRCh38#104952744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#8981500-C-A

104952744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8981500-C-T

104952780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8981489-C-T

104952789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-G

104952789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

104952790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-A

104952790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -G-T

104952852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8981428-C-G

104952852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8981428-C-T

104952856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8981424-G-A

104952856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8981424-G-C

104952856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8981424-G-T

104952863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8981422-A-G

104952864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 8981421-C-T

104952874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -A-G

http://identifiers.org/hco/14/GRCh38#104952955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#8981349-C-A

http://identifiers.org/hco/14/GRCh38#104952970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -A-C

104952970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -A-G

104952970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -A-T

104952977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -T-C

104952977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -T-G

104952988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: -C-T

104952993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -A-G

104953031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

104953037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: -G-T

104953348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 8981055-A-G

104954053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748478-G-T

http://identifiers.org/hco/14/GRCh38#104954101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112748526-A-C

104954124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748549-T-C

104954125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748550-T-C

104954171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748590-T-C

104954293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748725-T-C

104954298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 112748730-G-A

104954298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748730-G-T

104954311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748743-C-G

104954323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748755-C-G

104954323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748755-C-T

104954383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748805-C-G

104954386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748808-G-A

104954386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748808-G-T

http://identifiers.org/hco/14/GRCh38#104954414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112748836-A-C

104954417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748839-C-T

104954426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748848-G-A

104954441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 112748863-G-T

104954470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748892-T-A

104954470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748892-T-C

104954490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748912-G-A

104954490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112748912-G-T

104954511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748930-C-G

104954511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748930-C-T

104954513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748932-G-T

104954522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748941-T-C

104954535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112748954-C-T

http://identifiers.org/hco/14/GRCh38#104954548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112748967-C-A

104954605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112749024-T-C

104954639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112749058-C-G

104954639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112749058-C-T

104954694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 112749110-G-A

http://identifiers.org/hco/14/GRCh38#104954707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112749123-C-A

104954707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112749123-C-G

104954707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112749123-C-T

104954855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749273-G-A

104954855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749273-G-C

104955006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112749376-T-C

104955007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112749377-C-T

104955011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112749381-A-T

104955151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749518-G-T

104955232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749560-C-T

104955325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749632-A-T

http://identifiers.org/hco/14/GRCh38#104955346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112749653-C-A

104955352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749659-G-A

104955352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112749659-G-T

http://identifiers.org/hco/14/GRCh38#104955405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112749710-C-A

104955405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112749710-C-T

104955476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112749776-A-G

104955570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112749870-T-C

104955640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112749940-C-T

104955654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112749954-G-A

104955701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750000-G-T

104955933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750170-G-A

104955933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750170-G-C

104955942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750179-G-A

104956060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750279-C-T

104956255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750416-C-T

104956301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750459-G-A

104956439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750518-A-G

104956442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750521-G-C

104956442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750521-G-T

104956444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750523-G-A

104956444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750523-G-T

104956447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750526-A-T

104956577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750598-G-A

104956580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 112750601-G-A

104956672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112750693-C-T

104956681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112750702-G-C

104956705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750725-T-A

104956721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750742-T-C

104956721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750742-T-G

104956739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750758-G-C

104956739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750758-G-T

104956753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750775-T-C

104956766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750794-G-T

104956789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750809-G-T

104956953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112750911-C-T

http://identifiers.org/hco/14/GRCh38#104957125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112751190-C-A

104957154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751231-A-G

104957287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751402-T-G

104957301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751408-T-C

104957340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751447-G-A

104957340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751447-G-C

104957340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751447-G-T

104957368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751471-A-G

104957388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751500-G-A

104957388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751500-G-T

104957440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112751551-G-A

104957552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751679-A-G

104957552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751679-A-T

http://identifiers.org/hco/14/GRCh38#104957629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112751755-C-A

104957629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112751755-C-T

104957760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751858-T-A

http://identifiers.org/hco/14/GRCh38#104957810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112751874-A-C

104957810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751874-A-G

104957870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751934-G-A

104957872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112751936-A-G

104957967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112752014-C-T

104958013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112752060-T-C

104958046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112752093-C-T

104958162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112752216-G-A

104967407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112756509-T-G

104967447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112756551-G-A

104967454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112756558-G-A

104967576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112756679-G-A

http://identifiers.org/hco/14/GRCh38#104967831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112756886-C-A

104967831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112756886-C-T

104967969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112756993-C-T

104967991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757014-C-T

104968023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757058-C-T

104968069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757101-G-A

http://identifiers.org/hco/14/GRCh38#104968136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112757175-C-A

104968136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757175-C-T

104968172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757208-A-G

104968198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757239-G-T

104968249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757264-C-T

104968254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757273-G-A

http://identifiers.org/hco/14/GRCh38#104968317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112757321-C-A

104968317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757321-C-T

104968334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757338-T-G

104968380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757368-G-A

104968380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757368-G-C

104968834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112757625-C-T

104969055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112757859-T-G

104969395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112758098-T-C

104969583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112758260-G-C

104969610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112758292-G-A

104969671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112758495-G-C

http://identifiers.org/hco/14/GRCh38#104969781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112758606-C-A

http://identifiers.org/hco/14/GRCh38#104970064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112758876-C-A

104970064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112758876-C-T

104970154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112758966-G-A

104970211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112759000-C-T

104970230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112759024-G-A

http://identifiers.org/hco/14/GRCh38#104970241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112759035-C-A

104970388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112759219-T-C

104970458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 112759315-A-G

104970458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 112759315-A-T

http://identifiers.org/hco/14/GRCh38#104970475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112759327-C-A

104970496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112759346-A-G

104970549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112759392-T-C

http://identifiers.org/hco/14/GRCh38#104970599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112759440-C-A

104970599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112759440-C-T

http://identifiers.org/hco/14/GRCh38#104970722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112759593-C-A

104970722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112759593-C-G

104970722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112759593-C-T

104970830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112759696-A-T

104971958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112760406-C-T

104972127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112760509-G-A

104972127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112760509-G-C

104972275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112760606-T-C

104972439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112760776-T-C

104972895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112761033-G-A

104972905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112761043-G-C

104972981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112761116-C-T

http://identifiers.org/hco/14/GRCh38#104973212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112761306-C-A

104973229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112761323-C-G

104973500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112761595-G-A

104973627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112761831-G-A

104973647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112761861-G-T

104973702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112761908-C-T

104973721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112761923-G-A

104973892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112762078-G-A

http://identifiers.org/hco/14/GRCh38#104974018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112762176-A-C

104974173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112762333-G-A

104974549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112762514-C-T

104974734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112762636-A-G

104974820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112762728-A-G

104975560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112763535-G-C

104975749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112763697-T-C

104975782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112763739-T-C

104975792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112763749-C-T

104975985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112763889-G-C

104976165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112764071-G-A

http://identifiers.org/hco/14/GRCh38#104976175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112764081-C-A

104976344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: 112764322-G-A

104976762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112764680-T-C

104976771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112764692-G-A

104977722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112765635-C-T

104977756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112765665-C-T

http://identifiers.org/hco/14/GRCh38#104977798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112765701-C-A

http://identifiers.org/hco/14/GRCh38#104978103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112766007-C-A

104978103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112766007-C-T

http://identifiers.org/hco/14/GRCh38#104978104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112766008-C-A

104978104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112766008-C-G

104978135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112766043-T-C

104978174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112766083-G-A

104978174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: intron variant
orthologous variants: 112766083-G-T

104978293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5 prime UTR variant
orthologous variants: 112766202-G-A

104978293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5 prime UTR variant
orthologous variants: 112766202-G-C

104978293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5 prime UTR variant
orthologous variants: 112766202-G-T

http://identifiers.org/hco/14/GRCh38#104978325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#112766233-C-A

104978325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 112766233-C-T

104978333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 112766237-G-A

104978333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 112766237-G-C

104978333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 112766237-G-T

104978334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5 prime UTR variant
orthologous variants: 112766238-C-G

104978334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20125
most severe consequence: 5 prime UTR variant
orthologous variants: 112766238-C-T